Protein concentrates and isolates, and processes for the production thereof

ABSTRACT

Protein concentrates and protein isolates, in addition to processes for the production of protein concentrates and protein isolates, are disclosed. In particular, the disclosure relates to the removal of fiber from an oilseed meal using low g-force centrifugation.

PRIORITY INFORMATION

This application is a continuation-in-part of U.S. application Ser. No.12/467,227, filed May 15, 2009, which claims the benefit of U.S.Provisional Application Nos. 61/053,858 and 61/099,783 filed on May 16,2008 and Sep. 24, 2008, respectively, and entitled PROCESS FOR THEPRODUCTION OF PROTEIN CONCENTRATES AND PROTEIN ISOLATES, the contents ofwhich of which are expressly incorporated herein by reference.

FIELD OF THE DISCLOSURE

The present disclosure relates to protein concentrates and proteinisolates comprising combinations of proteins, peptides and amino acids,as well as processes for their production. In particular, the disclosurerelates to a process for removing fiber from an oilseed meal to produceedible protein products.

BACKGROUND

Oilseeds typically contain from about 20 percent oil to about 50 percentoil by weight, with the percentages varying with the type of oilseed.Generally, the seed is pressed, with or without a prior heat treatmentstep, to obtain a pressed oil and a pressed seedcake. Generally, thepressed seedcake is then solvent extracted to remove or reduce theremaining oil. After removal of the solvent from the pressed seedcakeand drying of the seedcake, there generally remains a defatted meal,which contains from about 25% to about 55% of protein on a dry weightbasis.

Some defatted meals, depending upon the oilseed, contain a high amountof fiber, as well as other anti-nutritional factors and undesirablecompounds, such as glucosinolates, phytic acid or phytates, sinapine andsinigrin. The fiber and antinutritional factors present in the proteinrender the defatted meal unattractive for commercial uses.

In the case of canola defatted meal, one method of separating theprotein from the fiber, antinutritional factors and other undesirablecompounds has been to dissolve the canola protein in a high ionicstrength (i.e. high salt content) aqueous solution. This results in thecanola protein dissolving in the aqueous solution, while the fiber isinsoluble. However, the salt is difficult and uneconomical to remove andrecover from the resultant canola protein solution.

SUMMARY OF THE DISCLOSURE

Herein, a process for the production of protein concentrates and proteinisolates is disclosed. In addition, protein concentrates and proteinisolates produced in accordance with the processes of the disclosure arealso disclosed. In particular, the disclosure relates to a process forthe facile removal of fiber, antinutritional factors and otherconstituents from an oilseed meal containing such, to produce proteinconcentrates and protein isolates of high quality.

In an embodiment of processes of the present disclosure, an oilseed isheat treated to a temperature of about 60° C. to about 120° C.,optionally about 70° C. to about 100° C., or about 80° C. to about 90°C., or about 80° C.

In another embodiment of the present disclosure, a process for theproduction of a protein concentrate possessing a protein content ofabout 70% to about 75% is disclosed.

Accordingly, the disclosure includes a process for the production of aprotein concentrate from a defatted or a protein-enriched meal,comprising:

-   -   1) removing fiber from the defatted or protein-enriched meal to        form a fiber depleted meal, comprising either:        -   i) mixing the defatted meal or protein-enriched meal with a            mixing solvent to form a first mixture; and            -   separating and removing fiber from the first mixture,                optionally by using a mesh screen; or            -   optionally treating the mixture with phytase at a                temperature and a pH suitable for phytase activity; or        -   ii) mixing the defatted or protein-enriched meal with water            to form a second mixture; and            -   optionally adjusting the pH of the second mixture to a                pH suitable for enzyme activity, optionally about 3 to                about 7, optionally 4 to 6; and            -   adding cellulase complex or other enzyme having fiber                hydrolysis activity to the second mixture and heating to                a temperature suitable for enzyme activity, to hydrolyze                the fiber;            -   optionally treating the mixture with phytase at a                temperature and a pH suitable for phytase activity,    -   2) washing the fiber depleted meal with an extraction solvent to        form an extract and a washed defatted or protein-enriched meal;    -   3) separating the extract from the washed defatted or        protein-enriched meal;    -   4) optionally repeating steps 2) and 3) at least once; and    -   5) optionally desolventizing the washed defatted or        protein-enriched meal to form a protein concentrate.

In another embodiment, the defatted or protein-enriched meal comprises acanola, rapeseed, mustard seed, broccoli seed, flax seed, cotton seed,hemp seed, safflower seed, sesame seed or soybean meal. In a furtherembodiment, the protein-enriched meal comprises a canola meal. In anembodiment, the protein-enriched meal comprises a soybean meal. Inanother embodiment, the protein-enriched meal comprises mustard seedmeal. In a further embodiment, the protein-enriched meal comprises flaxseed meal.

In another embodiment, the mixing solvent comprises water, methanol,ethanol or isopropanol, and mixtures thereof. In a further embodiment,the solvent is water or ethanol, and mixtures thereof. In an embodimentof the disclosure, the defatted or protein-enriched meal is mixed with amixing solvent in a ratio of about 3 to about 10 parts solvent to about1 part of the defatted or protein-enriched meal, optionally about 4 toabout 8, or about 4 to about 6, on a weight-to-weight basis.

In another embodiment of the disclosure, the mixture is screened througha mesh screen of typically about 10 to about 200 US mesh size,optionally a mesh screen of about 20 to about 200 US mesh size. Inanother embodiment, the mesh size is 40 US mesh size.

In an embodiment of the present disclosure, the defatted orprotein-enriched meal is mixed thoroughly with water to form the secondmixture. In an embodiment, the mixing of water and the defatted orprotein-enriched meal comprises using a wet mill or an inline mixer.

In another embodiment of the present disclosure, the cellulase complexis added to the second mixture in an amount of about 1 gram to about 10grams for about every 1 kg of dry solids of the defatted orprotein-enriched meal (about 0.1% to about 1%). In a further embodiment,the cellulase complex is mixed with the second mixture for about 0.5hours to about 5 hours. In another embodiment, the cellulase complex ismixed with the second mixture for about 1 to about 3 hours.

In another embodiment of the disclosure, the second mixture with theadded cellulase complex is heated to a temperature of about 30° C. toabout 60° C., suitably about 40° C. to about 60° C.

In an embodiment, the cellulase complex comprises at least one ofendocellulase, exocellulase, cellobiohydrolase, cellobiase,endohemicellulase and exohemicellulase.

In an embodiment of the disclosure, the extraction solvent comprisesmethanol, ethanol or isopropanol, and mixtures thereof. In a furtherembodiment, the extraction solvent comprises ethanol or water, andmixtures thereof.

In an embodiment of the present disclosure, the first or second mixtureis washed at least once with about 5% to about 100%, optionally about25% to about 85%, or about 50% to about 85%, or about 60% to about 85%,of the extraction solvent (v/v) in water.

In an embodiment of the present disclosure, the ratio of the extractionsolvent to the first or second mixture is about 5% to about 95%,optionally about 10% to about 90%, about 20% to about 70%, or about 40%to about 80% (v/v) (extraction solvent to first or second mixture).

In an embodiment of the present disclosure, the first or second mixtureis washed with the extraction solvent at a temperature of about 10° C.to about 90° C. In another embodiment, the first or second mixture iswashed with the extraction solvent at a temperature of about 20° C. toabout 60° C. In a further embodiment, the first or second mixture iswashed with the extraction solvent at a temperature of about 20° C. toabout 25° C.

In another embodiment of the present disclosure, the extract isseparated from the washed defatted or protein-enriched meal bycentrifugation, vacuum filtration, pressure filtration, decantation orgravity draining in an extractor.

In another embodiment of the present disclosure, steps 2) and 3) arerepeated at least twice.

In another embodiment of the present disclosure, the process furthercomprises the step of drying the washed defatted or protein-enrichedmeal to form the protein concentrate. In a further embodiment, thewashed defatted or protein-enriched meal is dried in a vacuum dryer,fluidized bed dryer, ring dryer or spray dryer. In another embodiment,the washed defatted or protein-enriched meal is dried to a moisturecontent of about 0.5% to about 12%, optionally about 1% to about 10%,about 4% to about 8%. In a further embodiment, the washed defatted orprotein-enriched meal is dried to a moisture content of about 6%.

In another embodiment of the present disclosure, the extract isdesolventized and dried to form a high sugar fraction. In an embodiment,the extract is desolventized by spray drying, drum drying or vacuumdrying.

In an embodiment of the present disclosure, a process for the productionof a protein concentrate possessing a protein content of about 75% toabout 90% is disclosed. In another embodiment, the protein concentrateis hydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein concentrate comprises peptides and/orfree amino acids.

The disclosure also includes a process for the production of a proteinconcentrate from a defatted or protein-enriched meal, comprising:

removing fiber from the defatted or protein-enriched meal, comprising:

-   -   i) mixing the defatted or protein-enriched meal with a mixing        solvent to form a mixture;        -   separating fiber from the mixture, optionally by screening            the mixture to remove fiber,        -   optionally adjusting the pH of the mixture to a pH of about            4.5 to about 8.0, optionally about 6.5 to about 7.5, or            optionally about 7;        -   optionally treating the mixture with phytase at a            temperature and a pH suitable for phytase activity,        -   optionally milling the mixture;        -   separating fiber, optionally by centrifuging the mixture, to            remove fiber,    -    thereby forming a protein slurry; and    -   ii) separating the protein slurry, optionally by centrifuging        the protein slurry, to form a protein precipitate and a soluble        protein fraction;    -   iii) washing the protein precipitate with an extraction solvent        at least once and separating, optionally by centrifuging, to        form a purified protein precipitate;    -   iv) optionally drying the purified protein precipitate to form        the protein concentrate.

In another embodiment, the defatted or protein-enriched meal comprises acanola, rapeseed, mustard seed, broccoli seed, flax seed, cotton seed,hemp seed, safflower seed, sesame seed or soybean meal. In a furtherembodiment, the protein-enriched meal comprises a canola meal. In anembodiment, the protein-enriched meal comprises a soybean meal. Inanother embodiment, the protein-enriched meal comprises mustard seedmeal. In a further embodiment, the protein-enriched meal comprises flaxseed meal.

In another embodiment of the disclosure, the mixing solvent compriseswater, methanol, ethanol, or isopropanol, and mixtures thereof. In afurther embodiment, the mixing solvent comprises water or ethanol, andmixtures thereof. In another embodiment, the ratio of defatted orprotein-enriched meal to the mixing solvent is about 1:3 to about 1:20.In a further embodiment, the ratio is about 1:6 to about 1:10. In anembodiment, the ratio is about 1:6 to about 1:8.

In another embodiment of the disclosure, the mixture is screened througha mesh screen of typically about 10 to about 200 US mesh size,optionally a mesh screen of about 20 to about 200 US mesh size. Inanother embodiment, the mesh size is 40 US mesh size.

In another embodiment of the present disclosure, the pH of mixture isadjusted with aqueous sodium hydroxide. In an embodiment, the aqueoussodium hydroxide has a concentration of about 1% to about 40% by weightof sodium hydroxide. In a further embodiment, the concentration ofsodium hydroxide is about 5% to about 30% sodium hydroxide.

In another embodiment, the optional milling step comprises using a wetmill.

In an embodiment, the mixture is centrifuged using a decantingcentrifuge. In an embodiment, the mixture is centrifuged with adecanting centrifuge at a speed of about 500 rpm to about 6000 rpm. Inanother embodiment, the speed is about 1500 rpm.

In an embodiment of the disclosure, the protein slurry is centrifugedusing a decanter or disc stack centrifuge. In a further embodiment, theprotein slurry is centrifuged at a speed of about 2500 rpm to about 8500rpm.

In another embodiment of the disclosure, the extraction solvent iswater, methanol, ethanol or isopropanol, and mixtures thereof. In afurther embodiment, the extraction solvent is water or ethanol, andmixtures thereof. In an embodiment, the extraction solvent is water. Inan embodiment, the protein precipitate is washed at least twice with theextraction solvent.

In an embodiment of the present disclosure, the washed proteinprecipitate is centrifuged with a disc stack centrifuge at a speed ofabout 7500 rpm to about 8500 rpm.

In an embodiment of the disclosure, the purified protein precipitate isdried in a vacuum dryer, fluidized bed dryer, ring dryer or spray dryerto form the protein concentrate. In a further embodiment, the proteinconcentrate is dried to a moisture content of about 1% to about 10%. Inanother embodiment, the protein concentrate is dried to a moisturecontent of about 6%.

In another embodiment, the protein concentrate comprises a hydrolyzedprotein concentrate. In another embodiment, the protein concentrate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein concentrate comprises peptides and/orfree amino acids.

In another embodiment of the present disclosure, a process for theproduction of a protein isolate possessing a protein content of greaterthan about 90% is disclosed.

Accordingly, the disclosure includes a process for the production of aprotein isolate from a defatted or protein-enriched meal, comprising:

removing fiber from the defatted or protein-enriched meal, comprising:

-   -   i) mixing the defatted or protein-enriched meal with a mixing        solvent to form a mixture;        -   separating fiber from the mixture to remove fiber,            optionally adjusting the pH of the mixture to a pH of about            6.0 to about 8.0, optionally about 6.5 to about 7.5, or            optionally about 7;        -   optionally milling the mixture;        -   optionally treating the mixture with phytase at a            temperature        -   and a pH suitable for phytase activity,        -   separating fiber, optionally by centrifuging the mixture, to            remove fiber,    -   thereby forming a protein slurry;    -   ii) separating the protein slurry, optionally by centrifuging        the protein slurry, to form a protein precipitate and a soluble        protein fraction;    -   iii) filtering the soluble protein fraction to separate it from        protein precipitate; and    -   iv) optionally drying the soluble protein to form the protein        isolate.

In another embodiment, the defatted or protein-enriched meal comprises acanola, rapeseed, mustard seed, broccoli seed, flax seed, cotton seed,hemp seed, safflower seed, sesame seed or soybean meal. In a furtherembodiment, the protein-enriched meal comprises a canola meal. In anembodiment, the protein-enriched meal comprises a soybean meal. Inanother embodiment, the protein-enriched meal comprises mustard seedmeal. In a further embodiment, the protein-enriched meal comprises flaxseed meal.

In another embodiment of the disclosure, the mixing solvent compriseswater or a salt solution. In an embodiment, the salt solution comprisesless than 5%, optionally about 3% to about 4%, or 3.5% by weight of saltin solution. In a further embodiment, the mixing solvent compriseswater. In another embodiment, the ratio of defatted or protein-enrichedmeal to the mixing solvent is about 1:3 to about 1:20. In a furtherembodiment, the ratio is about 1:6 to about 1:10. In an embodiment, theratio is about 1:6 to about 1:8.

In another embodiment of the present disclosure, the pH of mixture isadjusted with aqueous sodium hydroxide. In an embodiment, the aqueoussodium hydroxide has a concentration of about 1% to about 40% by weightof sodium hydroxide. In a further embodiment, the concentration ofsodium hydroxide is about 5% to about 30% sodium hydroxide.

In another embodiment of the disclosure, the mixture is screened througha mesh screen of about 10 to about 200 US mesh size, optionally a meshscreen of about 20 to about 200 US mesh size. In an embodiment, the meshsize is 40 US mesh size.

In an embodiment, the mixture is centrifuged using a decantingcentrifuge. In an embodiment, the mixture is centrifuged with adecanting centrifuge at a speed of about 500 rpm to about 6000 rpm. Inanother embodiment, the speed is about 1500 rpm.

In another embodiment, the optional milling step comprises using a wetmill.

In an embodiment of the disclosure, the protein slurry is centrifugedusing a disc stack centrifuge. In a further embodiment, the proteinslurry is centrifuged at a speed of about 6500 rpm to about 8500 rpm.

In another embodiment of the disclosure, the soluble protein fraction isfiltered using an ultrafiltration or diafiltration apparatus. In afurther embodiment, the ultrafiltration or diafiltration apparatuscomprises a membrane to filter proteins of larger than about 1,000daltons, optionally 10,000 daltons, optionally about 30,000 daltons, orabout 100,000 daltons. In another embodiment, the ultrafiltration ordiafiltration is performed at a temperature of about 1° C. to about 60°C., optionally about 40° C. to about 55° C.

In another embodiment of the disclosure, the soluble protein is dried ina vacuum dryer, fluidized bed dryer, ring dryer or spray dryer to formthe protein isolate. In an embodiment, the protein isolate is dried to amoisture content of about 1% to about 10%. In a further embodiment, theprotein isolate is dried to a moisture content of about 6%.

In another embodiment, the protein isolate comprises a hydrolyzedprotein isolate. In another embodiment, the protein isolate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein isolate comprises peptides and/orfree amino acids.

In another embodiment of the present disclosure, a process for theproduction of a protein isolate possessing a protein content of greaterthan about 90% is disclosed.

Accordingly, the disclosure includes a process for the production of aprotein isolate from a defatted or protein-enriched meal, comprising:

removing fiber from the defatted or protein-enriched meal, comprising:

-   -   i) mixing the defatted or protein-enriched meal with a mixing        solvent to form a mixture;        -   separating fiber from the mixture to remove fiber,        -   optionally adjusting the pH of the mixture to a pH of about            6.0 to about 8.0, optionally about 6.5 to about 7.5, or            optionally about 7;        -   optionally milling the mixture;        -   optionally treating the mixture with phytase at a            temperature and a pH suitable for phytase activity,        -   separating fiber, optionally by centrifuging the mixture, to            remove fiber,    -   thereby forming a protein slurry; and    -   ii) separating the protein slurry, optionally by centrifuging        the protein slurry, to form a protein precipitate and a soluble        protein fraction;    -   iii) mixing the protein precipitate with water to form a protein        precipitate mixture and optionally adjusting the pH to a pH        suitable for enzyme activity, optionally about 3 to about 7,        optionally about 4 to about 6;    -   iv) adding cellulase complex or other enzyme having fiber        hydrolysis activity to the protein precipitate mixture to        hydrolyze fiber, typically residual fiber;    -   v) washing the protein precipitate mixture with an extraction        solvent at least once and separating, optionally by        centrifuging, to form a protein isolate.

In another embodiment, the defatted or protein-enriched meal comprises acanola, rapeseed, mustard seed, broccoli seed, flax seed, cotton seed,hemp seed, safflower seed, sesame seed or soybean meal. In a furtherembodiment, the protein-enriched meal comprises a canola meal. In anembodiment, the protein-enriched meal comprises a soybean meal. Inanother embodiment, the protein-enriched meal comprises mustard seedmeal. In a further embodiment, the protein-enriched meal comprises flaxseed meal.

In another embodiment of the disclosure, the mixing solvent compriseswater or a salt solution. In an embodiment, the salt solution comprisesless than 5%, optionally about 3% to about 4%, or 3.5% by weight of saltin solution. In a further embodiment, the mixing solvent compriseswater. In another embodiment, the ratio of defatted or protein-enrichedmeal to the mixing solvent is about 1:3 to about 1:20. In a furtherembodiment, the ratio is about 1:6 to about 1:10. In an embodiment, theratio is about 1:6 to about 1:8.

In another embodiment of the disclosure, the mixture is screened througha mesh screen of about 10 to about 200 US mesh size, optionally a meshscreen of about 20 to about 200 US mesh size. In another embodiment, themesh size is 40 US mesh size.

In another embodiment of the present disclosure, the pH of mixture isadjusted with aqueous sodium hydroxide. In an embodiment, the aqueoussodium hydroxide has a concentration of about 1% to about 40% by weightof sodium hydroxide. In a further embodiment, the concentration ofsodium hydroxide is about 5% to about 30% sodium hydroxide.

In another embodiment, the optional milling step comprises using a wetmill.

In an embodiment, the mixture is centrifuged using a decantingcentrifuge. In an embodiment, the mixture is centrifuged with adecanting centrifuge at a speed of about 500 rpm to about 6000 rpm. Inanother embodiment, the speed is about 1500 rpm.

In an embodiment of the disclosure, the protein slurry is centrifugedusing a disc stack centrifuge. In a further embodiment, the proteinslurry is centrifuged at a speed of about 6500 rpm to about 8500 rpm.

In another embodiment of the disclosure, the cellulase complex is addedto the protein precipitate mixture in an amount of about 0.1% to about1% by weight of the protein precipitate mixture. In a furtherembodiment, the cellulase complex is mixed with the protein precipitatemixture for about 0.5 hours to about 5 hours. In another embodiment, thecellulase complex is mixed with the protein precipitate mixture forabout 1 to about 3 hours. In a further embodiment, the cellulase complexcomprises at least one of endocellulase, exocellulase,cellobiohydrolase, cellobiase, endohemicellulase and exohemicellulase.In an embodiment, the protein precipitate mixture with cellulase complexis heated to a temperature of about 30° C. to about 60° C. optionallyabout 40° C. to about 60° C.

In another embodiment of the disclosure, the mixing solvent compriseswater. In another embodiment, the ratio of defatted or protein-enrichedmeal to the mixing solvent is about 1:3 to about 1:20. In a furtherembodiment, the ratio is about 1:6 to about 1:10. In an embodiment, theratio is about 1:6 to about 1:8.

In another embodiment of the present disclosure, the protein precipitatemixture is centrifuged using a decanter or disc stack centrifuge. In afurther embodiment, the protein precipitate mixture is centrifuged at aspeed of about 2500 rpm to about 8500 rpm.

In another embodiment of the present disclosure, the protein isolate issubjected to high pressure jet cooking.

In an embodiment of the present disclosure, the protein isolate ishydrolyzed using proteases to form a hydrolyzed protein extract. In afurther embodiment, the proteases comprise Alcalase® (serineendopeptidase, typically from Bacillus subtilis), or Flavourzyme®(fungal protease/peptidase complex, typically produced from Aspergillusoryzae fermentation), both proteases from Novozymes® North America, Inc.In an embodiment, the ratio of Alcalase® to the protein isolate is about0.1% to about 1%. In another embodiment, the ratio of Alcalase® to theprotein isolate is about 0.5%. In a further embodiment, the ratio ofFlavourzyme® to the protein isolate is about 0.1% to about 1%. In anembodiment, the ratio of Flavourzyme® to the protein isolate is about0.5%.

In another embodiment, the protein isolate comprises a hydrolyzedprotein isolate. In another embodiment, the protein isolate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein isolate comprises peptides and/orfree amino acids.

In another embodiment of the disclosure, there is a provided a processfor the production of a protein concentrate from an oilseed meal,comprising:

-   -   i) mixing the partially defatted, fully defatted or        protein-enriched meal with a mixing solvent to form a mixture        and optionally treating the mixture with phytase at a        temperature and a pH suitable for phytase activity,    -   ii) optionally adjusting the pH of the mixture to a pH of about        2.0 to about 10.0;    -   iii) separating fiber from the mixture to form a protein slurry,        wherein the protein slurry comprises a soluble protein fraction        and an insoluble protein fraction;    -   iv) optionally repeating steps i)-iii) by mixing the protein        slurry with additional partially defatted, fully defatted or        protein-enriched meal;    -   v) mixing the protein slurry with an extraction solvent to form        an extract and a washed insoluble protein fraction;    -   vi) separating the extract from the washed insoluble protein        fraction;    -   vii) optionally repeating steps v) and vi) at least once; and    -   viii) optionally desolventizing the washed insoluble protein        fraction to form a protein concentrate.

In another embodiment of the disclosure, the ratio of partiallydefatted, fully defatted or protein-enriched meal to mixing solvent isabout 1:3 to about 1:30 (w/w). In another embodiment, the ratio ofpartially defatted, fully defatted or protein-enriched meal to solventis about 1:5 to about 1:20 (w/w). In a further embodiment, the ratio isabout 1:6 to about 1:12 (w/w). In an embodiment, the ratio is about 1:8to about 1:10 (w/w).

In a further embodiment of the disclosure, the mixing solvent compriseswater or an aqueous solution comprising a polysaccharide, a salt, suchas sodium chloride, potassium chloride, or calcium chloride, or analcohol. In an embodiment, the mixing solvent is water. In anotherembodiment, the polysaccharide is guar gum.

In an embodiment, the pH of the protein slurry is adjusted to a pH ofabout 6.5 to about 10.0. In a further embodiment, the pH of the proteinslurry is adjusted to a pH of about 7.0 to about 9.0.

In another embodiment of the disclosure, the mixture is separated bycentrifugation or hydrocyclone to separate the fiber from the mixtureand form the protein slurry. In a further embodiment, the mixture isseparated by centrifugation to separate the fiber from the mixture andform the protein slurry. In an embodiment, the mixture is centrifuged ata speed of about 1,000 rpm to about 2,000 rpm. In a further embodiment,the mixture is centrifuged at a speed of about 1,400 to about 1,600 rpm.In an embodiment, the mixture is centrifuged using a decantercentrifuge.

In another embodiment of the disclosure, mixing the protein slurry withadditional partially defatted, fully defatted or protein-enriched mealis repeated at least once. In a further embodiment, mixing the proteinslurry with additional partially defatted, fully defatted orprotein-enriched meal is repeated at least two to seven times.

In an embodiment of the disclosure, the extraction solvent compriseswater, methanol, ethanol, isopropanol, or mixtures thereof. In anembodiment, the extraction solvent comprises ethanol. In anotherembodiment, the extraction solvent comprises at least about 50% ethanol.In an embodiment, the extraction solvent comprises at least about 70%ethanol. In a further embodiment, the extraction solvent comprises atleast about 90% ethanol.

In a further embodiment, the extract is separated from the washedinsoluble protein fraction using centrifugation, vacuum filtration,pressure filtration, decantation or gravity draining. In an embodiment,the extract is separated from the washed insoluble protein fractionusing centrifugation.

In another embodiment of the disclosure, wherein steps iv) and v) arerepeated at least twice.

In a further embodiment, the process further comprises the step ofdrying the washed insoluble protein fraction to form the proteinconcentrate. In an embodiment, the protein concentrate is dried in avacuum dryer, fluidized bed dryer, hot air dryer ring dryer or spraydryer.

In another embodiment, the protein concentrate comprises a hydrolyzedprotein concentrate. In another embodiment, the protein concentrate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein concentrate comprises peptides and/orfree amino acids.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched meal comprises a canola, rapeseed, mustardseed, broccoli seed, flax seed, cotton seed, hemp seed, safflower seed,sesame seed or soybean meal. In another embodiment, the partiallydefatted, fully defatted or protein-enriched meal comprises a canolameal.

In an embodiment, the protein concentrate comprises a protein content ofabout 60% to about 90% on a dry weight basis.

In another embodiment of the disclosure, there is also provided aprocess for the production of a protein isolate from an oilseed meal,comprising:

-   -   i) mixing the partially defatted, fully defatted or        protein-enriched meal with a blending solvent, optionally water        or alkaline water, to form a mixture and optionally treating the        mixture with phytase at a temperature and a pH suitable for        phytase activity;    -   ii) optionally adjusting the pH of the mixture to a pH of about        7.0 to about 10.0;    -   iii) separating fiber from the mixture to form a first protein        slurry, wherein the first protein slurry comprises a soluble        protein fraction and an insoluble protein fraction;    -   iv) separating the first protein slurry to form a protein solids        fraction and a soluble protein fraction;    -   v) optionally mixing the protein solids fraction with a second        blending solvent, optionally water, to form a second protein        slurry;    -   vi) optionally separating the second protein slurry to form a        second protein solids fraction and a second soluble protein        fraction;    -   vii) optionally repeating steps v) and vi) at least once;    -   viii) separating the soluble protein fractions to form a        clarified soluble protein fraction and a residual insoluble        protein fraction;    -   ix) optionally adjusting the pH of the clarified soluble protein        fraction to a pH of about 6 to about 9;    -   x) separating the clarified soluble protein fraction, optionally        by filtering the clarified soluble protein fraction by membrane        filtration; and    -   xi) optionally drying the clarified soluble protein fraction.

In another embodiment of the disclosure, the ratio of partiallydefatted, fully defatted or protein-enriched meal to water or alkalinewater is about 1:4 to about 1:30 (w/w). In another embodiment, the ratioof partially defatted, fully defatted or protein-enriched meal to wateror alkaline water is about 1:5 to about 1:20 (w/w). In a furtherembodiment, the ratio is about 1:6 to about 1:12 (w/w). In anembodiment, the ratio is about 1:8 to about 1:10 (w/w).

In an embodiment of the disclosure, the pH of the alkaline water isabout 7 to about 12. In another embodiment, the pH of the first proteinslurry is adjusted to about 8.0 to about 9.5. In a further embodiment,the pH of the first protein slurry is adjusted to about 8.5 to about9.0.

In another embodiment of the disclosure, the mixture is separated bycentrifugation or hydrocyclone to separate the fiber from the mixtureand form the protein slurry. In a further embodiment, the mixture isseparated by centrifugation to separate the fiber from the mixture andform the protein slurry. In an embodiment, the mixture is centrifuged ata speed of about 1,000 rpm to about 2,000 rpm. In a further embodiment,the mixture is centrifuged centrifuge at a speed of about 1,400 to about1,600 rpm. In an embodiment, the mixture is centrifuged using a decantercentrifuge.

In another embodiment, the first protein slurry is centrifuged,optionally using a disc stack centrifuge, to separate the protein solidsfraction from the soluble protein fraction. In a further embodiment, thefirst protein slurry is centrifuged at a speed of about 4,000 rpm toabout 8,000 rpm. In a further embodiment, the first protein slurry iscentrifuged at a speed of about 6,500 to about 7,500 rpm.

In another embodiment of the disclosure, the ratio of the protein solidsfraction to water is about 1.0:0.5 to about 1.0:3.0 (w/w). In a furtherembodiment, the ratio of the protein solids fraction to water is about1.0:1.0 to about 1.0:2.0 (w/w).

In an embodiment, the soluble protein fractions are centrifuged to formthe clarified soluble protein fraction and the residual insolubleprotein fraction. In an embodiment, the soluble protein fractions arecentrifuged using a disc stack centrifuge at a speed of about 7,000 rpmto about 10,000 rpm. In a further embodiment, the soluble proteinfractions are centrifuged using a disc stack centrifuge at a speed ofabout 7,500 rpm to about 8,500 rpm.

In another embodiment of the disclosure, the pH of the clarified solubleprotein fraction is adjusted with alkali. In a further embodiment, thepH of the clarified soluble protein fraction is adjusted with sodiumhydroxide.

In an embodiment, the clarified soluble protein fraction is filteredusing an ultrafiltration apparatus. In a further embodiment, theultrafiltration apparatus comprises a membrane to filter proteins largerthan about 10,000 daltons.

In another embodiment of the disclosure, the process further comprisesthe step of filtering the clarified soluble protein fraction using adiafiltration apparatus.

In another embodiment, the clarified soluble protein fraction is driedin a vacuum dryer, fluidized bed dryer, ring dryer or spray dryer toform the protein isolate.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched meal comprises a canola, rapeseed, mustardseed, broccoli seed, flax seed, cotton seed, hemp seed, safflower seed,sesame seed or soybean meal. In another embodiment, the partiallydefatted, fully defatted or protein-enriched meal comprises a canolameal.

In another embodiment, the protein isolate comprises a hydrolyzedprotein isolate. In another embodiment, the protein isolate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein isolate comprises peptides and/orfree amino acids.

In another embodiment of the disclosure, the protein isolate comprises aprotein content of greater than about 90% on a dry weight basis.

In another embodiment of the disclosure, there is also provided aprocess for the production of a hydrolyzed protein concentrate from anoilseed meal, comprising:

-   -   i) mixing the oilseed meal with a blending solvent, optionally        water, to form a first mixture and optionally treating the        mixture with phytase at a temperature and a pH suitable for        phytase activity;    -   ii) optionally adjusting the pH of the first mixture to a pH of        about 6.5 to about 10.0;    -   iii) separating the first mixture to remove fiber from the first        mixture and form a protein slurry and an insoluble fiber        fraction, wherein the protein slurry comprises a soluble protein        fraction and an insoluble protein fraction and the insoluble        fiber fraction comprises insoluble fiber and a second insoluble        protein fraction;    -   iv) optionally mixing the insoluble fiber fraction with a second        blending solvent, optionally water, to form a washed insoluble        fiber fraction and an extract;    -   v) separating the washed insoluble fiber fraction from the        extract;    -   vi) optionally mixing the washed insoluble fiber fraction with a        blending solvent, optionally water, to form a second mixture;    -   vii) optionally adjusting the pH of the second mixture to a pH        suitable for enzymatic activity;    -   viii) mixing the second mixture with at least one protease to        form a hydrolyzed protein extract;    -   ix) separating the hydrolyzed protein extract from the second        mixture to form the hydrolyzed protein concentrate and a second        insoluble fiber fraction; and    -   x) optionally drying the hydrolyzed protein concentrate.

In another embodiment of the disclosure, the ratio of partiallydefatted, fully defatted or protein-enriched meal to water is about 1:4to about 1:30 (w/w).

In another embodiment, the ratio of partially defatted, fully defattedor protein-enriched meal to water is about 1:5 to about 1:20 (w/w). In afurther embodiment, the ratio is about 1:6 to about 1:12 (w/w). In anembodiment, the ratio is about 1:8 to about 1:10 (w/w).

In another embodiment, the pH of the first mixture is adjusted to about8.0 to about 9.5. In a further embodiment, the pH of the first mixtureis adjusted to about 8.5 to about 9.0.

In another embodiment of the disclosure, the first mixture is separatedby centrifugation or hydrocyclone to separate the fiber from the firstmixture and form the protein slurry. In a further embodiment, themixture is separated by centrifugation to separate the fiber from themixture and form the protein slurry. In an embodiment, the first mixtureis centrifuged at a speed of about 1,000 rpm to about 2,000 rpm. In afurther embodiment, the first mixture is centrifuged centrifuge at aspeed of about 1,400 to about 1,600 rpm. In an embodiment, the mixtureis centrifuged using a decanter centrifuge.

In another embodiment, the ratio of the insoluble fiber fraction orwashed insoluble fiber fraction to water is about 1.0:0.5 to about1.0:3.0 (w/w). In a further embodiment, the ratio of the insoluble fiberfraction or washed insoluble fiber fraction to water is about 1.0:1.0 toabout 1.0:2.0 (w/w).

In another embodiment, the washed insoluble fiber fraction iscentrifuged to separate the washed insoluble fiber fraction fromextract. In a further embodiment, the washed insoluble fiber fraction iscentrifuged at a speed of about 2,000 rpm to about 6,000 rpm. In afurther embodiment, washed insoluble fiber fraction is centrifuged at aspeed of about 3,000 to about 5,500 rpm.

In another embodiment of the disclosure, the pH of the second mixture isadjusted to about 8.0 to about 9.0.

In an embodiment of the disclosure, the ratio of the second mixture tothe protease is about 100:1 to about 5000:1 (w/w).

In an embodiment of the disclosure, the second mixture is mixed with aprotease at a temperature of about 40° C. to about 60° C. In anotherembodiment, the second mixture is mixed with a protease at a temperatureof about 45° C. to about 55° C.

In another embodiment, the at least one protease comprises a proteasefrom Bacillus Licheniformis.

In a further embodiment, the process further comprises the step ofmixing the second mixture with a second protease.

In an embodiment, the ratio of the second mixture to the second proteaseis about 250:1 to about 5000:1 (w/w).

In another embodiment, the second mixture is mixed with the secondprotease at a temperature of about 50° C. to about 70° C. In anembodiment, the second mixture is mixed with the second protease at atemperature of about 55° C. to about 65° C.

In a further embodiment, the second protease comprises a fungalprotease/peptidase complex from Aspergillus oryzae.

In another embodiment, the hydrolyzed protein concentrate is dried in avacuum dryer, fluidized bed dryer, ring dryer or spray dryer to form theprotein isolate.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched meal comprises a canola, rapeseed, mustardseed, broccoli seed, flax seed, cotton seed, hemp seed, safflower seed,sesame seed or soybean meal. In another embodiment, the partiallydefatted, fully defatted or protein-enriched meal comprises a canolameal.

In a further embodiment, the hydrolyzed protein concentrate comprises aprotein content of about 60% to about 90% on a dry weight basis.

In another embodiment, the process further comprises mixing thehydrolyzed protein extract with water to form a third mixture. In afurther embodiment, the process further comprises filtering the thirdmixture fraction and the filtering comprises ultrafiltration. In anembodiment, the ultrafiltration comprises contacting the third mixturewith an ultrafiltration apparatus that comprises a membrane to filterproteins larger than about 1,000 daltons.

In another embodiment, the process further comprises mixing the secondinsoluble fiber fraction to form a washed hydrolyzed protein extract anda washed second insoluble fiber fraction and separating the form thewashed hydrolyzed protein extract from the washed second insoluble fiberfraction. In another embodiment, the washed hydrolyzed protein extractis combined with the hydrolyzed protein extract.

In an embodiment of the disclosure, there is also provided a process forthe production of a protein concentrate from an oilseed meal comprising:

-   -   i) mixing the oilseed meal with a blending solvent, optionally        water, a saline solution or a polysaccharide solution, to form a        mixture and optionally treating the mixture with phytase at a        temperature and a pH suitable for phytase activity;    -   ii) optionally adjusting the pH of the mixture to a pH of about        2.0 to about 10.0;    -   iii) separating fiber from the mixture to form a protein slurry,        wherein the protein slurry comprises a first soluble protein        fraction and an insoluble protein fraction;    -   iv) optionally repeating steps i)-iii) by mixing the protein        slurry with additional oilseed meal;    -   v) separating the soluble protein fraction from the insoluble        protein fraction;    -   vi) washing the insoluble protein fraction with a second        blending solvent, optionally water, saline solution or        polysaccharide solution, to form a washed insoluble protein        fraction and a second soluble protein fraction;    -   vii) separating the washed insoluble protein fraction and the        second soluble protein fraction;    -   viii) combining and separating the first and second soluble        protein fractions to form a protein concentrate, optionally by        filtering the first and second soluble protein fractions to form        a protein concentrate or isolate;    -   ix) combining the washed insoluble protein fraction with the        protein concentrate to form a combined protein concentrate or        isolate; and    -   x) optionally drying the combined protein concentrate.

In another embodiment of the disclosure, the ratio of partiallydefatted, fully defatted or protein-enriched meal to water is about 1:3to about 1:30 (w/w). In another embodiment, the ratio of partiallydefatted, fully defatted or protein-enriched meal to water is about 1:5to about 1:20 (w/w). In a further embodiment, the ratio is about 1:6 toabout 1:12 (w/w). In an embodiment, the ratio is about 1:8 to about 1:10(w/w).

In an embodiment, the pH of the mixture is adjusted to a pH of about 6.5to about 10.0. In another embodiment, the pH of the mixture is adjustedto a pH of about 7.0 to about 9.0.

In another embodiment of the disclosure, the mixture is separated bycentrifugation or hydrocyclone to separate the fiber from the mixtureand form the protein slurry. In a further embodiment, the mixture isseparated by centrifugation to separate the fiber from the mixture andform the protein slurry. In an embodiment, the mixture is centrifuged ata speed of about 1,000 rpm to about 2,000 rpm. In a further embodiment,the mixture is centrifuged at a speed of about 1,400 to about 1,600 rpm.In an embodiment, the mixture is centrifuged using a decantercentrifuge.

In another embodiment, the protein slurry is centrifuged to separate theprotein solids fraction from the soluble protein fraction. In anembodiment, the protein slurry is centrifuged at a speed of about 6,000rpm to about 8,500 rpm in a disc stack centrifuge. In anotherembodiment, the protein slurry is centrifuged at a speed of about 6,500to about 7,500 rpm.

In another embodiment, the ratio of the insoluble protein fraction towater is about 1.0:0.5 to about 1.0:3.0 (w/w). In a further embodiment,the ratio of the insoluble protein fraction to water is about 1.0:1.0 toabout 1.0:2.0 (w/w).

In another embodiment, the washed insoluble protein fraction and thesecond soluble protein fraction are separated using a centrifuge. In anembodiment, the washed insoluble protein fraction and the second solubleprotein fraction are centrifuged at a speed of about 6,000 rpm to about8,500 rpm in a disc stack centrifuge. In a further embodiment, thewashed insoluble protein fraction and the second soluble proteinfraction are centrifuged at a speed of about 6,500 to about 7,500 rpm.

In another embodiment, the first and second soluble protein fractionsare filtered using an ultrafiltration apparatus. In a furtherembodiment, the ultrafiltration apparatus comprises a membrane to filterproteins larger than about 10,000 daltons. In an embodiment, the processfurther comprises the step of filtering the first and second solubleprotein fractions using a diafiltration apparatus.

In another embodiment, the combined protein concentrate is dried in avacuum dryer, fluidized bed dryer, ring dryer or spray dryer to form thedried protein concentrate.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched meal comprises a canola, rapeseed, mustardseed, broccoli seed, flax seed, cotton seed, hemp seed, safflower seed,sesame seed or soybean meal. In another embodiment, the partiallydefatted, fully defatted or protein-enriched meal comprises a canolameal.

In another embodiment, the protein concentrate comprises a hydrolyzedprotein concentrate. In another embodiment, the protein concentrate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein concentrate comprises peptides and/orfree amino acids.

In a further embodiment, the protein concentrate comprises a proteincontent of about 60% to about 90% on a dry weight basis.

In an embodiment of the disclosure, there is also provided a process forthe production of a protein isolate from an oilseed meal comprising:

-   -   i) mixing the oilseed meal with a blending solvent, optionally        water, to form a mixture and optionally treating the mixture        with phytase at a temperature and a pH suitable for phytase        activity;    -   ii) optionally adjusting the pH of the mixture to a pH of about        2.0 to about 10.0;    -   iii) separating fiber from the mixture to form a protein slurry,        wherein the protein slurry comprises a soluble protein fraction        and an insoluble protein fraction;    -   iv) washing the fiber with a second blending solvent, optionally        water, to form a washed fiber fraction;    -   vi) separating the washed fiber fraction to form a second        protein slurry and washed fiber solids;    -   vii) combining and separating the first and second protein        slurries to form a protein concentrate, optionally by filtering        the first and second soluble protein fractions to form a protein        concentrate; and    -   ix) optionally drying the protein concentrate.

In another embodiment of the disclosure, the ratio of partiallydefatted, fully defatted or protein-enriched meal to water is about 1:3to about 1:30 (w/w). In another embodiment, the ratio of partiallydefatted, fully defatted or protein-enriched meal to water is about 1:5to about 1:20 (w/w). In a further embodiment, the ratio is about 1:6 toabout 1:12 (w/w). In an embodiment, the ratio is about 1:8 to about 1:10(w/w).

In an embodiment, the pH of the mixture is adjusted to a pH of about 6.5to about 10.0. In another embodiment, the pH of the mixture is adjustedto a pH of about 7.0 to about 9.0.

In another embodiment of the disclosure, the mixture is separated bycentrifugation or hydrocyclone to separate the fiber from the mixtureand form the protein slurry. In a further embodiment, the mixture isseparated by centrifugation to separate the fiber from the mixture andform the protein slurry. In an embodiment, the mixture is centrifuged ata speed of about 1,000 rpm to about 2,000 rpm. In a further embodiment,the mixture is centrifuged centrifuge at a speed of about 1,400 to about1,600 rpm. In an embodiment, the mixture is centrifuged using a decantercentrifuge.

In another embodiment, the ratio of the fiber fraction to water is about1.0:0.5 to about 1.0:3.0 (w/w). In a further embodiment, the ratio ofthe insoluble protein fraction to water is about 1.0:1.0 to about1.0:2.0 (w/w).

In another embodiment of the disclosure, the washed fiber fraction isseparated by centrifugation, gravity sedimentation, a gravity table orhydrocyclone to separate the fiber solids and form second the proteinslurry. In a further embodiment, the washed fiber fraction is separatedby centrifugation to separate the fiber and form the second proteinslurry. In an embodiment, the mixture is centrifuged at a speed of about1,000 rpm to about 2,000 rpm. In a further embodiment, the fiberfraction is centrifuged centrifuge at a speed of about 1,400 to about1,600 rpm. In an embodiment, the fiber fraction is centrifuged using adecanter centrifuge.

In another embodiment, the first and second slurries are filtered usingan ultrafiltration/microfiltration apparatus. In a further embodiment,the ultrafiltration/microfiltration apparatus comprises a membrane tofilter proteins larger than about 10,000 daltons. In an embodiment, theprocess further comprises the step of filtering the first and secondslurries using a diafiltration apparatus.

In another embodiment, the protein concentrate is dried in a vacuumdryer, fluidized bed dryer, ring dryer or spray dryer to form the driedprotein concentrate.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched meal comprises a canola, rapeseed, mustardseed, broccoli seed, flax seed, cotton seed, hemp seed, safflower seed,sesame seed or soybean meal. In another embodiment, the partiallydefatted, fully defatted or protein-enriched meal comprises a canolameal.

In another embodiment, the protein isolate comprises a hydrolyzedprotein isolate. In another embodiment, the protein isolate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein isolate comprises peptides and/orfree amino acids.

In a further embodiment, the protein concentrate comprises a proteincontent of about 60% to about 90% on a dry weight basis.

In another embodiment of the disclosure, there is also provided aprocess for the removal of fiber from a partially defatted, fullydefatted or protein-enriched meal, comprising:

-   -   i) mixing an oilseed meal with a blending solvent, optionally        water, an aqueous solution or protein containing solution, to        form a mixture and optionally treating the mixture with phytase        at a temperature and a pH suitable for phytase activity;    -   ii) optionally adjusting the pH of the protein slurry to a pH of        about 2 to about 10; and    -   iii) separating the mixture to form a protein slurry comprising        soluble and insoluble proteins and an insoluble fiber fraction.

In another embodiment of the disclosure, there is also included proteinconcentrates and protein isolates, produced in accordance with theprocesses of the disclosure. Accordingly, in an embodiment of thedisclosure, there is provided an oilseed protein isolate having aprotein content of at least 90% (w/w), wherein the canola proteinisolate has a solubility of at least 85% (w/w), wherein the solubilityis measured at a concentration of about 1% and a pH of about 6.5 toabout 7.5 in a borate-phosphate buffer solution. In another embodiment,the oilseed protein isolate has a solubility of at least 95% (w/w) in aborate-phosphate buffer solution. In a further embodiment, the oilseedprotein isolate has a solubility of at least 99% (w/w) in aborate-phosphate buffer solution. In a further embodiment, the oilseedprotein isolate has a solubility of at least 99.5% (w/w) in aborate-phosphate buffer solution.

In another embodiment of the disclosure, the oilseed protein isolate hasa solubility of at least 85% (w/w) at a concentration of about 1% and apH of about 6.5 to about 7.0 in a borate-phosphate buffer solution. In afurther embodiment, the oilseed protein isolate has a solubility of atleast 85% (w/w) at a concentration of about 1% and a pH of about 6.7 toabout 7.0 in a borate-phosphate buffer solution.

In another embodiment of the disclosure, the oilseed protein isolate hasa solubility of at least 85% (w/w) at a concentration of about 1% and apH of about 6.5 to about 7.0 in a borate-phosphate buffer solution at atemperature of about 35° C. to about 45° C. In another embodiment of thedisclosure, the oilseed protein isolate has a solubility of at least 85%(w/w) at a concentration of about 1% and a pH of about 6.5 to about 7.0in a borate-phosphate buffer solution at a temperature of about 38° C.to about 40° C.

In another embodiment, the oilseed protein isolate comprises,

i) a first class of proteins having a molecular weight of about 60 kDato about 80 kDa, the first class of proteins comprising about 60% toabout 90% (w/w) of the oilseed isolate;

ii) a second class of proteins having a molecular weight of about 10 kDato about 30 kDa, the second class of proteins comprising about 10% toabout 30% (w/w) of the oilseed isolate; and

iii) a third class of proteins having a molecular weight of less thanabout 10 kDa, the third class of proteins comprising about 2% to about10% (w/w) of the oilseed isolate.

In another embodiment, the oilseed protein isolate comprises,

i) a first class of proteins having a molecular weight of about 60 kDato about 80 kDa, the first class of proteins comprising about 60% toabout 70% (w/w) of the oilseed isolate;

ii) a second class of proteins having a molecular weight of about 10 kDato about 30 kDa, the second class of proteins comprising about 20% toabout 30% (w/w) of the oilseed isolate; and

iii) a third class of proteins having a molecular weight of less thanabout 10 kDa, the third class of proteins comprising about 5% to about10% (w/w) of the oilseed isolate.

In a further embodiment, the oilseed protein isolate comprises

i) a first class of proteins having a molecular weight of about 65 kDato about 75 kDa, the first class of proteins comprising about 60% toabout 90% (w/w) of the oilseed isolate;

ii) a second class of proteins having a molecular weight of about 10 kDato about 20 kDa, the second class of proteins comprising about 10% toabout 30% (w/w) of the oilseed isolate; and

iii) a third class of proteins having a molecular weight of less thanabout 10 kDa, the third class of proteins comprising about 2% to about10% (w/w) of the oilseed isolate.

In another embodiment, the oilseed protein isolate comprises

i) a first class of proteins having a molecular weight of about 65 kDato about 70 kDa, the first class of proteins comprising about 60% toabout 70% (w/w) of the oilseed isolate;

ii) a second class of proteins having a molecular weight of about 10 kDato about 20 kDa, the second class of proteins comprising about 20% toabout 30% (w/w) of the oilseed isolate; and

iii) a third class of proteins having a molecular weight of less thanabout 10 kDa, the third class of proteins comprising about 5% to about10% (w/w) of the oilseed isolate.

In another embodiment of the disclosure, the oilseed protein isolatecomprises a canola, rapeseed, mustard seed, broccoli seed, flax seed,cotton seed, hemp seed, safflower seed, sesame seed or soybean oilseedprotein isolate. In another embodiment, the oilseed comprises a canolaoilseed.

In another embodiment, the oilseed protein isolate has anantinutritional concentration less than about 0.5% (w/w), optionallyless than 0.1%. In a further embodiment, the oilseed protein isolate hasa threonine content of at least about 4.1% (w/w) and a valine content ofat least about 5.1% (w/w).

In another embodiment of the disclosure, there is also included aoilseed protein hydrolyzate having a protein content of about 60% toabout 90% and having a protein dispersibility index of at least 95.0%and wherein a 1.0% solution (w/w) in water of the protein hydrolyzatehas a visible light transmittance of least 90.0%. In a furtherembodiment, the oilseed protein hydrolyzate has a protein dispersibilityindex of at least 99.0%. In an embodiment, the oilseed proteinhydrolyzate has a protein dispersibility index of at least 99.8%.

In another embodiment of the disclosure, a 1.0% solution (w/w) of theprotein hydrolyzate has a visible light transmittance of least 95.0%. Ina further embodiment, a 1.0% solution (w/w) of the protein hydrolyzatehas a visible light transmittance of least 97.0%. In an embodiment, theoilseed protein hydrolyzate contains less than 1% by weight of fiber.

In another embodiment, the oilseed protein hydrolyzate has anantinutritional concentration less than about 0.5% (w/w). In a furtherembodiment, the oilseed protein hydrolyzate has a threonine content ofat least about 4.1% (w/w), a valine content of at least about 5.1%(w/w), a methionine content of at least about 1.7% (w/w) and anisoleucine content of at least about 5.0% (w/w).

In another embodiment of the disclosure, there is also included anoilseed protein concentrate having a protein content of about 60% toabout 90%, wherein the protein has a methionine content at least 1.90%by weight and a cysteine content at least 1.60% by weight. In anembodiment, the oilseed protein concentrate has a methionine content atleast 1.95% by weight. In an embodiment, the oilseed protein concentratehas a methionine content at least 2.02% by weight. In an embodiment, theoilseed protein concentrate has a cysteine content at least 1.65% byweight. In an embodiment, the oilseed protein concentrate has a cysteinecontent at least 1.68% % by weight.

In another embodiment, the protein concentrate further has a threoninecontent of at least 4.0% by weight, a valine content of at least 5.1%(w/w) and a luecine content of at least 8.25% (w/w) of the total proteinweight. In another embodiment, the oilseed protein concentrate has anantinutritional concentration less than about 0.5% (w/w), optionallyless than 0.1%.

In another embodiment, the protein concentrate has a glucosinolatecontent of less than about 1 μmol/g of the protein concentrate, andoptionally less than about 0.5 μmol/g.

The present disclosure relates to processes for the production ofprotein concentrates and protein isolates, in addition to hydrolyzedprotein concentrates and isolates, in which the toasted oilseed meal issubjected to low g-forces to separate the fiber from the insoluble andsoluble protein fractions.

Accordingly, the present disclosure includes a process for theproduction of a protein concentrate from an oilseed meal comprising:

i) mixing the oilseed meal with a first blending solvent to form amixture;

ii) optionally treating the mixture with phytase at a temperature and apH suitable for phytase activity;

iii) optionally adjusting the pH of the mixture to a pH between 6.0 and10.0;

iv) subjecting the mixture to a g-force sufficient to separate themixture to form

-   -   a) a fiber fraction, and    -   b) protein fractions comprising an insoluble protein fraction        and a soluble protein fraction;

v) optionally mixing the fiber fraction with a second blending solventand repeating step iv);

vi) optionally adjusting the pH of the protein fractions to a pH between4.0 and 6.0;

vii) optionally heating the protein fractions to a temperature between80° C. and 100° C. to precipitate the proteins; and

viii) separating the precipitated proteins from the protein fraction toform the protein concentrate.

In another embodiment, the first and second blending solvents comprisewater, a saline solution or a polysaccharide solution. In a furtherembodiment, the first and second blending solvents comprise water.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched oilseed meal comprises a canola, rapeseed,mustard seed, broccoli seed, flax seed, cotton seed, hemp seed,safflower seed, sesame seed or soybean meal. In another embodiment, thepartially defatted, fully defatted or protein-enriched oilseed mealcomprises a canola meal.

In an embodiment of the disclosure, the ratio of the oilseed meal to thefirst blending solvent is 1:3 to 1:30 (w/w) of meal to water, optionallyabout 1:8 to about 1:10 (w/w).

In an embodiment of the disclosure, the phytase is added in an amountbetween 0.01% and 0.1% (w/w) based on the weight of the oilseed meal. Ina further embodiment, the temperature suitable for phytase activity isbetween 20° and 60° C. In a further embodiment, the pH suitable forphytase activity is between 2.0 and 7.0.

In another embodiment of the disclosure, the mixture is subjected to ag-force of between 100 g and 500 g, optionally between 150 g and 400 g,suitably between 180 g and 350 g.

In another embodiment, separating the mixture comprises using acentrifuge or a hydrocyclone. In another embodiment, the centrifugecomprises a decanter centrifuge or disc stack centrifuge.

In a further embodiment, separating the precipitated proteins comprisesusing a centrifuge or a hydrocyclone. In another embodiment, separatingthe precipitated proteins comprises using a centrifuge. In anotherembodiment, centrifuging the precipitated proteins comprises a g-forcebetween 2,500 g and 9,500 g.

In another embodiment of the disclosure, the process further comprisesthe step of drying the protein concentrate to a moisture content ofbetween 4% and 8% (w/w).

In another embodiment, the protein concentrate comprises a hydrolyzedprotein concentrate. In another embodiment, the protein concentrate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein concentrate comprises peptides and/orfree amino acids.

In another embodiment, there is also included a protein concentratehaving a protein content of at least 60% and less than 90% proteincomprising:

i) a first protein fraction comprising between 30% and 70% 2S protein;

ii) a second protein fraction comprising between 20% and 50% 12Sprotein.

The present disclosure also includes a process for the production of aprotein concentrate from an oilseed meal comprising:

i) mixing the oilseed meal with a first blending solvent to form amixture;

ii) optionally treating the mixture with phytase at a temperature and apH suitable for phytase activity;

iii) optionally adjusting the pH of the mixture to a pH between 6.0 and10.0;

iv) subjecting the mixture to a g-force sufficient to separate themixture to form

-   -   a) a fiber fraction, and    -   b) protein fractions comprising an insoluble protein fraction        and a soluble protein fraction;

v) optionally mixing the fiber fraction with a second blending solventand repeating step iv);

vi) optionally adjusting the pH of the protein fractions to a pH between4.0 and 6.0;

vii) mixing the protein fractions with a mixing solvent to form aprotein slurry and precipitate the proteins;

viii) separating the precipitated proteins from the protein slurry toform the protein concentrate; and

viii) optionally repeating steps vi) and vii) with the precipitatedproteins.

In another embodiment, the first and second blending solvents comprisewater, a saline solution or a polysaccharide solution. In a furtherembodiment, the first and second blending solvents comprise water.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched oilseed meal comprises a canola, rapeseed,mustard seed, broccoli seed, flax seed, cotton seed, hemp seed,safflower seed, sesame seed or soybean meal. In another embodiment, thepartially defatted, fully defatted or protein-enriched oilseed mealcomprises a canola meal.

In an embodiment of the disclosure, the ratio of the oilseed meal to thefirst blending solvent is 1:3 to 1:30 (w/w) of meal to water, optionallyabout 1:8 to about 1:10 (w/w).

In an embodiment of the disclosure, the phytase is added in an amountbetween 0.01% and 0.1% (w/w) based on the weight of the oilseed meal. Ina further embodiment, the temperature suitable for phytase activity isbetween 20° and 60° C. In a further embodiment, the pH suitable forphytase activity is between 2.0 and 7.0.

In another embodiment of the disclosure, the mixture is subjected to ag-force of between 100 g and 500 g, suitably between 150 g and 400 g,optionally between 180 g and 350 g.

In another embodiment, separating the mixture comprises using acentrifuge or a hydrocyclone. In another embodiment, the centrifugecomprises a decanter centrifuge or a disc stack centrifuge.

In another embodiment of the disclosure, the mixing solvent comprises anethanol:water mixture, wherein the ethanol is present in an amountbetween 90% and 100% (v/v).

In another embodiment, separating the precipitated proteins comprisesusing a centrifuge or a hydrocyclone. In another embodiment, separatingthe precipitated proteins comprises using a centrifuge. In anotherembodiment, centrifuging the precipitated proteins comprises a g-forcebetween 2,500 g and 9,500 g.

In another embodiment of the disclosure, steps vii) and viii) arerepeated at least twice.

In another embodiment, the process further comprises the step of dryingthe protein concentrate to a moisture content of between 4% and 8%(w/w).

In another embodiment, the protein concentrate comprises a hydrolyzedprotein concentrate. In another embodiment, the protein concentrate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein concentrate comprises peptides and/orfree amino acids.

In another embodiment, there is also included a protein concentratehaving a protein content of at least 60% and less than 90% proteincomprising:

i) a first protein fraction comprising between 30% and 70% 2S protein;

ii) a second protein fraction comprising between 20% and 50% 12Sprotein.

The present disclosure also includes a process for the production of aprotein isolate from an oilseed meal comprising:

i) mixing the oilseed meal with a first blending solvent to form amixture;

ii) optionally treating the mixture with phytase at a temperature and apH suitable for phytase activity;

iii) optionally adjusting the pH of the mixture to a pH between 6.0 and10.0;

iv) subjecting the mixture to a g-force sufficient to separate themixture to form

-   -   a) a fiber fraction, and    -   b) protein fractions comprising an insoluble protein fraction        and a soluble protein fraction;

v) optionally mixing the fiber fraction with a second blending solventand repeating step iv);

vi) separating the insoluble protein fraction from the soluble proteinfraction to recover therefrom an insoluble protein concentrate and asoluble protein extract; and

vii) subjecting the soluble protein extract to filtration to recovertherefrom the protein isolate.

In another embodiment, the first and second blending solvents comprisewater, a saline solution or a polysaccharide solution. In a furtherembodiment, the first and second blending solvents comprise water.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched oilseed meal comprises a canola, rapeseed,mustard seed, broccoli seed, flax seed, cotton seed, hemp seed,safflower seed, sesame seed or soybean meal. In another embodiment, thepartially defatted, fully defatted or protein-enriched oilseed mealcomprises a canola meal.

In an embodiment of the disclosure, the ratio of the oilseed meal to thefirst blending solvent is 1:3 to 1:30 (w/w) of meal to water, optionallyabout 1:8 to about 1:10 (w/w).

In an embodiment of the disclosure, the phytase is added in an amountbetween 0.01% to 0.1% (w/w) based on the weight of the oilseed meal. Ina further embodiment, the temperature suitable for phytase activity isbetween 20° and 60° C. In a further embodiment, the pH suitable forphytase activity is between 2.0 and 7.0.

In another embodiment of the disclosure, the mixture is subjected to ag-force of between 100 g and 500 g, suitably between 150 g and 400 g,optionally between 180 g and 350 g.

In another embodiment, separating the mixture comprises using acentrifuge or a hydrocyclone. In an embodiment, the centrifuge comprisesa decanter centrifuge or a disc stack centrifuge.

In another embodiment, separating the insoluble protein fraction fromthe soluble protein fraction comprises using a centrifuge or ahydrocyclone. In a further embodiment separating the insoluble proteinfraction from the soluble protein fraction comprises using a centrifuge.In another embodiment, centrifuging to separate the insoluble proteinfraction from the soluble protein fraction comprises a g-force between2,500 g and 9,500 g.

In another embodiment, the process further comprises the step of dryingthe protein isolate to a moisture content of between 4% and 8% (w/w).

In another embodiment, the protein isolate comprises a hydrolyzedprotein isolate. In another embodiment, the protein isolate ishydrolyzed to produce peptides and free amino acids. In anotherembodiment, the hydrolyzed protein isolate comprises peptides and/orfree amino acids.

In another embodiment, there is also included a protein isolate having aprotein content of at least 90% protein comprising:

i) a first protein fraction comprising between 10% and 40% 2S protein;

ii) a second protein fraction comprising between 30% and 70% 12Sprotein.

Other features and advantages of the present disclosure will becomeapparent from the following detailed description. It should beunderstood, however, that the detailed description and the specificexamples while indicating preferred embodiments of the disclosure aregiven by way of illustration only, since various changes andmodifications within the spirit and scope of the disclosure will becomeapparent to those skilled in the art from this detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the invention will be described in relation to thedrawings in which:

FIG. 1 is a schematic representation showing a preparation of defattedmeal of an oilseed;

FIG. 2 is a schematic representation showing a preparation of aprotein-enriched meal from the defatted meal of an oilseed;

FIG. 3 is schematic representation showing a preparation of a proteinconcentrate from a protein-enriched meal;

FIG. 4 is a schematic representation of a first embodiment showing theremoval of fiber during a preparation of a protein concentrate from aprotein-enriched meal;

FIG. 5 is a schematic representation of a second embodiment showing theremoval of fiber during a preparation of a protein concentrate from aprotein-enriched meal;

FIG. 6 is a schematic representation of a third embodiment showing theremoval of fiber during a preparation of a protein concentrate from aprotein-enriched meal;

FIG. 7 is a schematic representation of a fourth embodiment showing theremoval of fiber during the preparation of a protein concentrate from aprotein-enriched meal;

FIG. 8 is a schematic representation of a first embodiment showing apreparation of a protein concentrate and a protein isolate from aprotein-enriched meal;

FIG. 9 is a schematic representation of a second embodiment showing apreparation of a protein concentrate and a protein isolate from aprotein-enriched meal;

FIG. 10 is a schematic representation of a first embodiment showing apreparation of a protein isolate from a protein-enriched meal;

FIG. 11 is a schematic representation of a second embodiment showing apreparation of a protein isolate from a protein-enriched meal;

FIG. 12 is a schematic representation of a first embodiment for crushingof Juncea Seed and preparation of defatted Juncea meal;

FIG. 13 is a schematic representation of a first embodiment showing apreparation of a protein concentrate from a protein enriched meal;

FIG. 14 is a schematic representation of a second embodiment showing apreparation of a protein concentrate from a protein enriched meal;

FIG. 15 is a schematic representation of a third embodiment showing apreparation of a protein concentrate from a protein enriched meal;

FIG. 16 is a schematic representation of a second embodiment showing thecrushing of Juncea seed and preparation of defatted Juncea meal;

FIG. 17 is a schematic representation showing the milling and screeningof defatted Juncea meal;

FIG. 18 is a schematic representation illustrating a separation andremoval of fiber from a protein slurry containing insoluble and solubleproteins;

FIG. 19 is a schematic representation illustrating a preparation of aprotein concentrate from a protein slurry with fiber removed;

FIG. 20 is a schematic representation illustrating a preparation of aprotein isolate and a hydrolyzed protein extract;

FIG. 21 is a schematic representation illustrating a preparation of ahydrolyzed protein extract;

FIG. 22 is a schematic representation illustrating a wet fiber removalprocess;

FIG. 23 is a schematic representation illustrating a milling andscreening process of defatted Juncea meal;

FIG. 24 is a schematic representation illustrating a separation andremoval of fiber from a protein slurry containing insoluble and solubleproteins;

FIG. 25 is a schematic representation illustrating a preparation of aprotein concentrate from a protein slurry after the removal of fiber;

FIG. 26 is a schematic representation illustrating a preparation of ahydrolyzed protein concentrate;

FIG. 27 is a schematic representation illustrating a wet fiber removalprocess;

FIG. 28 is a schematic representation illustrating a first recycling ofa protein fraction and a wet fiber removal process;

FIG. 29 is a schematic representation illustrating a second recycling ofa protein fraction and a wet fiber removal process;

FIG. 30 is a schematic representation illustrating a third recycling ofa protein fraction and a wet fiber removal process;

FIG. 31 is a schematic representation illustrating a fourth recycling ofa protein fraction and a wet fiber removal process;

FIG. 32 is a schematic representation illustrating a fifth recycling ofa protein fraction and a wet fiber removal process;

FIG. 33 is schematic representation illustrating a preparation of aprotein concentrate produced by recycling a protein fraction;

FIG. 34 is a schematic representation of a first embodiment illustratinga preparation of a protein concentrate;

FIG. 35 is a schematic representation of a second embodimentillustrating a preparation of a protein concentrate;

FIG. 36 is a graph showing the foam volume of a protein isolate producedin accordance with a process of the present disclosure;

FIG. 37 is a graph showing the gel forming temperature of a proteinisolate produced in accordance with a process of the present disclosure;

FIG. 38 is a graph showing the oscillation tests of gels of a proteinisolate produced in accordance with a process of the present disclosure;

FIG. 39 is a graph showing the oscillation test of gels of differentconcentrations of a protein isolate produced in accordance with aprocess of the present disclosure;

FIG. 40 is a schematic representation of a first embodiment showing theremoval of fiber during the preparation of a protein concentrate from adefatted meal;

FIG. 41 is a schematic representation of a second embodiment showing theremoval of fiber during the preparation of a protein concentrate from adefatted meal;

FIG. 42 is a schematic representation showing the removal of fiberduring the preparation of a protein concentrate and a protein isolatefrom a defatted meal;

FIG. 43 is a graph showing sedimentation velocity of proteins in aprotein isolate;

FIG. 44 is a graph showing sedimentation velocity of proteins in aprotein concentrate; and

FIG. 45 is a graph showing sedimentation velocity of proteins in ahydrolyzed protein concentrate.

DETAILED DESCRIPTION OF THE DISCLOSURE (I) Definitions

The term “peptide” as used herein refers to various natural compoundscontaining two or more amino acids linked by the carboxylic acid groupof one amino acid to the amino group of another amino acid. Peptidesgenerally have 4-100 amino acids (US Patent Office Classification IndexGlossary) and a molecular weight of less than about 10,000 Daltons.

The term “protein” as used herein refers to peptides with more thanabout 50-100 amino acids and a molecular weight in excess of about10,000 Daltons. The US Patent Office Classification Index Glossarydefines protein as peptides with more then 100 amino acids.

The term “partially defatted meal” (alternatively called “seedcake” or“presscake”) as used herein refers to an oilseed meal in which theoilseed has been pressed to remove the oil contained within. Thepressing of the oilseed results in pressed oil and a partially defattedmeal, which contains from about 15% to about 50% of protein on a dryweight basis and from about 10% to about 20% oil, optionally about 14%to 16%, on a dry weight basis.

The term “defatted meal” (alternatively called “fully defatted meal”) asused herein refers to an oilseed which has been ii) pressed to removeoil, which forms a seedcake and pressed oil, and ii) subjected tosolvent extraction, using, for example, hydrophobic and low-boilingsolvents, such as butane, pentane, hexane and/or other refrigerants suchas iodotrifluoromethane (ITFM) and R134a (1,1,1,2-tetrafluoroethane), toremove or reduce residual oil from the seedcake and form the defattedmeal. A defatted meal will typically have a protein content of about 25%to about 55%, optionally 30% to about 50%, suitably about 35% to about50%, on a dry weight basis, and from about 0% to about 4% oil,optionally about 0.5% to about 4%, optionally about 1% to about 3%, on adry weight basis.

The term “protein-enriched meal” as used herein refers to a defattedmeal as described above, which has subsequently been treated to removefiber from the defatted meal. Accordingly, the defatted meal istypically subjected to a milling step and a screening step to removefiber and obtain a protein-enriched meal having a protein content ofabout 30% to about 60%, optionally 40% to 55%, suitably 50% to 55% on adry weight basis, and about 5% to about 6.5% fiber, optionally less thanabout 6%. Collectively, a partially defatted meal, fully defatted mealand a protein-enriched meal may be referred to as “meal”.

The term “protein concentrate” as used herein refers to a defatted orprotein-enriched meal that has been treated using the processes of thepresent disclosure to increase the protein content, where the proteinconcentrate has greater than 60% protein content but less than 90%protein content on a dry weight basis. The balance may comprisecarbohydrate, ash, fiber and oil. In an embodiment, the proteinconcentrate is generally produced from the insoluble protein fraction orsoluble/insoluble protein fractions of a protein mixture.

The term “hydrolyzed protein concentrate” as used herein refers to aprotein concentrate that has been treated to hydrolyze the proteinswithin the protein concentrate into amino acids and smaller peptides.Proteins can be hydrolyzed using various chemicals, such as strong acidsand bases, and enzymes, preferably proteases.

The term “protein isolate” as used herein refers to a defatted orprotein-enriched meal that has been treated using the processes of thepresent disclosure to increase the protein content, where the proteinisolate has 90% or greater than 90% protein on a dry weight basis. Thebalance may comprise carbohydrate, ash, and oil. In an embodiment, theprotein isolate is generally produced from the soluble protein fractionof a protein mixture.

The term “hydrolyzed protein isolate” as used herein refers to a proteinisolate that has been treated with proteases to hydrolyze the proteinswithin the protein isolate into amino acids and smaller peptides.

The term “mixing solvent” as used herein refers to a solvent that formsa protein slurry or mixture when mixed with a partially defatted, fullydefatted or protein-enriched meal. In addition, the fiber present in themeal possesses minimal solubility in the mixing solvent (e.g. typicallyless than 1% (w/w) solubility, or about 0% solubility), and suitably, isnot soluble in the mixing solvent. Examples of mixing solvents include,but are not limited to, water, alcohols, such as methanol, ethanol orisopropanol, polysaccharide solutions such as guar gum solution, salinesolutions, or mixtures of any of the above.

The term “blending solvent” as used herein refers to any aqueous solvent(typically at least: 80%, 85%, 90%, 95%, 98% or 99% water by weight)that forms a slurry or mixture when mixed with a partially defatted,fully defatted or protein-enriched meal. Typically the blending solventis free from organic solvents, such as methanol, ethanol, propanol,iso-propanol, tetrahydrofuran since these solvents are not desirable asresidues in a protein isolate, concentrate or hydroxylate for humanconsumption, however, if organic solvents are present, they are in theblending solvent in small amount (e.g. typically equal to or less than:20%, 10%, 10%, 5% or 1%) so that their presence in the final product isnegligible. Examples of blending solvents include water, acidic water,alkaline water, saline salt solutions (such as sodium chloride,potassium chloride, calcium chloride), polysaccharide solutions (such asguar gum), and aqueous protein solutions.

The invention contemplates using a variety of solvents, which couldinclude blending solvents, mixing solvents or other combinations oralcohols (e.g. 80% ethanol), water and/or aqueous solvents. The use ofthe term blending solvents should not be construed as precluding the useof organic solvents in processes as disclosed herein.

The term “extraction solvent” as used herein refers to a solvent whichis capable of solubilizing antinutritional compounds, or otherconstituents, that are present in the oilseed and which are desirablyremoved. Examples of antinutritionals include, but are not limited to,glucosinolates, phytic acid, phytates and other compounds that reducethe nutritional or commercial value of the protein concentrate orprotein isolate. Antinutritional compounds are compounds that are, forexample, not digestible by mammals (e.g. humans), have adverse effects,such as toxicity or are bitter tasting, and are desirably removed fromthe protein product. Accordingly, the concentration of antinutritionalsin a protein product produced in accordance with a process of thepresent disclosure is less than about 1% (w/w), optionally less thanabout 0.5% (w/w), optionally less than about 0.1% (w/w), and optionallyless than about 0.05% (w/w). Examples of other compounds include, butare not limited to, materials that undesirably effect the quality,color, taste, odor, appearance or characteristics of the end product.Examples include compounds that cause a darkening or variation in thecolor, cause a bitter taste or a pungent odor, such as sinapine orsinigrin, or affect the handling or agglomeration of the end product.While the antinutritionals or other components are not desirable in theprotein concentrates or isolates they may constitute commerciallyvaluable side products which can have utility as medicinal or industrialingredients or end products once separated from the protein concentrateor isolate. Examples of extraction solvents include, but are not limitedto, water, alcohols, such as methanol, ethanol, isopropanol, or mixturesof any of the above. Other extractions solvents which are useful includetetrahydrofuran (THF), dimethylformamide (DMF), and ethers, such asmethyl t-butyl ether. However, it will be known to those skilled in theart that solvents such as THF, DMF or ethers, as a result of theirhigher toxicity as compared to, for example, ethanol, require lowerlimits in the protein product.

The term “homogeneous agitation” as used herein refers to the mixing ofa protein meal, such as a partially defatted meal, a fully defatted mealor a protein-enriched meal with a solvent to form a homogenous mixtureor suspension. Such agitation is accomplished, for example, by mixingthe slurry or mixture at a speed of about 30 rpm to about 300 rpm in astandard mixer.

The term “washed” used herein refers to a protein fraction that has beenmixed with an extraction solvent, such as ethanol, to removeantinutritional compounds, or other constituents, from the proteinfraction.

The term “protein slurry” as used herein refers to protein, for example,the protein in a defatted or protein-enriched meal, that has been mixedwith a mixing solvent to form a suspension of protein, and optionallyfiber and other antinutritional compounds, in the mixing solvent.

The terms “soluble protein fraction” and “insoluble protein fraction” asused herein refer to specific protein fractions which are either solubleor insoluble, respectively, in a particular solvent, such as a blendingsolvent, mixing solvent or an extraction solvent. In an embodiment, theinsoluble protein fraction is generally composed of insoluble globulinand denatured proteins. The insoluble protein fraction is generallycomposed of insoluble globulin proteins. In another embodiment, thesoluble protein fraction is generally composed of albumin, solubleglobulin and undenatured proteins. The soluble protein fraction isgenerally composed of soluble albumin and soluble globulin proteins.

The term “water” as used herein refers to any source of water, forexample, tap water, distilled water or reverse osmosis water.

The term “alkaline water” as used herein refers to water which has abasic pH of greater than about 7.0, optionally about 7.0 to about 12.0.The alkalinity of the water results from the addition of a base towater, for example, an alkali hydroxide such as sodium hydroxide. Forexample, a solution of sodium hydroxide at a concentration of about 5%to about 15% (w/w), optionally 11%.

The term “suitable for phytase activity” as used herein refers to theconditions, such as the temperature and pH, and optionally includes thelength of time, in which the phytase enzyme is able to hydrolyze thephosphate groups on phytate or phytic acid, and accordingly, reduce theamount of phytates or phytic acid in the mixture. In an embodiment, thetemperature suitable for phytase activity is between 20° C. and 60° C.,optionally between 40° C. and 55° C., suitably between 50° C. and 55° C.In another embodiment, the pH suitable for phytase activity is between2.0 and 7.0, optionally between 4.0 and 6.0, suitably between 4.5 and5.5, optionally 5.0 to 5.5. In another embodiment, the concentration ofthe phytase enzyme is between 0.01% to 1.0% (w/w) based on the weight ofthe oilseed meal, optionally 0.01% and 0.5% optionally 0.01% and 0.1%.It will be understood that the conditions suitable for phytase activityapply to all of the processes of the present disclosure.

The term “g-force sufficient to separate the mixture to form a fiberfraction and a protein fraction comprising an insoluble protein fractionand a soluble protein fraction” as used herein refers to the forcenecessary to separate the insoluble fiber fraction in the mixture fromthe protein fractions. In an embodiment, the g-force is between 100 gand 500 g, suitably between 150 g and 400 g, optionally between 180 gand 350 g. It will be understood that when the mixture is subjected to asufficient g-force, the insoluble fiber, due to its relative higherdensity and/or greater particle size, will separate from the proteinfractions. It should also be recognized that forces greater than theranges necessary to separate the phases are not desirable as they canresult in the high concentrations of the insoluble protein beingdeposited in the fiber phase. In addition, as a result of the insolubleprotein fraction having a higher relative density and/or particle sizecompared to the soluble protein, the insoluble protein fraction willseparate from the soluble protein fraction. It will be understood thoughthat not all of the protein will separate from the insoluble fiberfraction, and likewise, not all of the insoluble fiber will separatefrom the protein fraction. Moreover, not all of the insoluble proteinfraction will separate from the soluble protein fraction. Accordingly,when the mixture has been subjected to a g-force sufficient to separatethe mixture, the insoluble fiber fraction will comprise at least 10%crude fiber, optionally 15%, 20%, 25, 30% crude fiber on a dry weightbasis. Likewise, the protein fraction will comprise less than 10% crudefiber, optionally less than 5%, 4%, 3%, 2%, 1% and less than 1% crudefiber with the majority of other material comprising soluble andinsoluble proteins, carbohydrate, ash and oil. In an embodiment, theg-force sufficient to separate the mixture is obtained by rotating acentrifuge at a speed of about 500 RPM to about 2,500 RPM. It will beunderstood that a centrifuge will have a rotational radius which willvary depending on the size of the centrifuge. In another embodiment, theg-force sufficient to separate the mixture is obtained by using ahydrocyclone with a g-force of between 50 g and 250 g.

(II) Protein Concentrates and Isolates

The present disclosure relates to processes for the production of aprotein concentrate or a protein isolate from oilseed. A proteinconcentrate is an isolated protein extract of pressed oilseed, whereinthe extract has greater than 60% protein content but less than 90%protein content on a dry weight basis. A protein concentrate has beentreated to separate protein in the oilseed from the fiber and otherunwanted antinutritional factors. A protein isolate is an isolatedprotein extract of pressed oilseed, wherein the extract has greater thanor equal to 90% protein content on a dry weight basis. Typically, theprotein isolate has up to 98%, 99%, 99.5% or 100% protein content on adry weight basis. Examples of pressed oilseed include seedcake, defattedmeal or protein-enriched meal, as explained below. Typically, thenon-protein content includes non-protein compounds such asantinutritional substances, fiber, and other components or impuritiessuch as coloring agents.

In an embodiment, the disclosure provides a process for the removal offiber, antinutritionals and other constituents, that are present withinthe oilseed. A person skilled in the art would recognize thatantinutritionals include glucosinolates, phytic acid, phytates and othercompounds that reduce the nutritional or commercial value of the proteinconcentrate or protein isolate. For example, antinutritional compoundsmay not be digestible by mammals (e.g. humans), have adverse effects,such as toxicity, and are desirably removed from the protein product.Certain antinutritionals have other undesirable properties, such asundesirable organoleptic properties. Examples of such compounds aresinapine, which has a bitter taste, and sinigrin which has a pungent andvery bitter flavor. Further, other antinutritional constituent ofoilseeds that are typically removed include, but are not limited to,coloring agents and/or other inert compounds. In an embodiment, theconstituents which are removed or are reduced to safe or acceptablelevels, are undesirable constituents or impurities using the processesof the present disclosure. A person skilled the art would recognize thesafe and/or acceptable levels of particular antinutritionals in thefinal protein product.

The term protein-enriched meal refers to a meal that possesses a proteincontent of about 30% to about 60%, optionally 30% to 55%, suitably 50%to 55%, on a dry weight basis. Such protein-enriched meals are useful toprepare the concentrates and isolates of the disclosure, which may befurther processed.

In another embodiment of the disclosure, there is also included proteinconcentrates and protein isolates, produced in accordance with theprocesses of the disclosure. Accordingly, in an embodiment of thedisclosure, there is provided an oilseed protein isolate having aprotein content of at least 90%, wherein the canola protein isolate hasa solubility of at least 85% (w/w) at a concentration of about 1% and apH of about 6.5 to about 7.5 in a borate-phosphate buffer solution. Inanother embodiment, the oilseed protein isolate has a solubility of atleast 95% (w/w) in a borate-phosphate buffer solution. In a furtherembodiment, the oilseed protein isolate has a solubility of at least 99%(w/w) in a borate-phosphate buffer solution. In a further embodiment,the oilseed protein isolate has a solubility of at least 99.5% (w/w) ina borate-phosphate buffer solution.

In another embodiment of the disclosure, the oilseed protein isolate hasa solubility of at least 85% (w/w) at a concentration of about 1% and apH of about 6.5 to about 7.0 in a borate-phosphate buffer solution. In afurther embodiment, the oilseed protein isolate has a solubility of atleast 85% (w/w) at a concentration of about 1% and a pH of about 6.7 toabout 7.0 in a borate-phosphate buffer solution.

In another embodiment of the disclosure, the oilseed protein isolate hasa solubility of at least 85% (w/w) at a concentration of about 1% and apH of about 6.5 to about 7.0 in a borate-phosphate buffer solution at atemperature of about 35° C. to about 45° C. In another embodiment of thedisclosure, the oilseed protein isolate has a solubility of at least 85%(w/w) at a concentration of about 1% and a pH of about 6.5 to about 7.0in a borate-phosphate buffer solution at a temperature of about 38° C.to about 40° C.

In another embodiment, the oilseed protein isolate comprises,

i) a first class of proteins having a molecular weight of about 60 kDato about 80 kDa, the first class of proteins comprising about 60% toabout 90% (w/w) of the oilseed isolate;

ii) a second class of proteins having a molecular weight of about 10 kDato about 30 kDa, the second class of proteins comprising about 10% toabout 30% (w/w) of the oilseed isolate; and

iii) a third class of proteins having a molecular weight of less thanabout 10 kDa, the third class of proteins comprising about 2% to about10% (w/w) of the oilseed isolate.

In another embodiment, the oilseed protein isolate comprises,

i) a first class of proteins having a molecular weight of about 60 kDato about 80 kDa, the first class of proteins comprising about 60% toabout 70% (w/w) of the oilseed isolate;

ii) a second class of proteins having a molecular weight of about 10 kDato about 30 kDa, the second class of proteins comprising about 20% toabout 30% (w/w) of the oilseed isolate; and

iii) a third class of proteins having a molecular weight of less thanabout 10 kDa, the third class of proteins comprising about 5% to about10% (w/w) of the oilseed isolate.

In a further embodiment, the oilseed protein isolate comprises

i) a first class of proteins having a molecular weight of about 65 kDato about 75 kDa, the first class of proteins comprising about 60% toabout 90% (w/w) of the oilseed isolate;

ii) a second class of proteins having a molecular weight of about 10 kDato about 20 kDa, the second class of proteins comprising about 10% toabout 30% (w/w) of the oilseed isolate; and

iii) a third class of proteins having a molecular weight of less thanabout 10 kDa, the third class of proteins comprising about 2% to about10% (w/w) of the oilseed isolate.

In another embodiment, the oilseed protein isolate comprises

i) a first class of proteins having a molecular weight of about 65 kDato about 70 kDa, the first class of proteins comprising about 60% toabout 70% (w/w) of the oilseed isolate;

ii) a second class of proteins having a molecular weight of about 10 kDato about 20 kDa, the second class of proteins comprising about 20% toabout 30% (w/w) of the oilseed isolate; and

iii) a third class of proteins having a molecular weight of less thanabout 10 kDa, the third class of proteins comprising about 5% to about10% (w/w) of the oilseed isolate.

In an embodiment of the disclosure, the protein isolate produced inaccordance with a process of the present disclosure contains greaterthan 90% protein content (w/w) on a dry weight basis, optionally 90% toabout 99% (w/w), optionally 90% to about 98% (w/w), and optionally 90%to about 95% (w/w). In another embodiment, a protein isolate produced inaccordance with a process of the present disclosure contains less thanabout 1% (w/w) fiber, optionally less than about 0.5% (w/w) fiber, andoptionally less than about 0.1% (w/w) fiber.

In another embodiment of the disclosure, the oilseed protein isolatecomprises a canola, rapeseed, mustard seed, broccoli seed, flax seed,cotton seed, hemp seed, safflower seed, sesame seed or soybean oilseedprotein isolate. In another embodiment, the oilseed comprises a canolaoilseed.

In an embodiment of the disclosure, oilseed protein isolates, such as acanola protein isolate, produced in accordance with the processes of thepresent disclosure, have excellent emulsifying and foaming properties.For example, with respect to emulsifying capacity, a 0.5% (w/w) canolaprotein isolate solution possessed a similar emulsifying capacity ascompared to a 5% egg yolk solution. Further, the protein isolates of thepresent disclosure, such as a canola protein isolate, possess excellentfoaming capacity. Further, oilseed protein isolates, such as a canolaprotein isolate, produced in accordance with the processes of thepresent disclosure, have excellent properties of gel formation and waterimmobilization, and therefore, act as stabilizers.

In another embodiment of the disclosure, there is also included aoilseed protein hydrolyzate having a protein content of about 60% toabout 90% and having a protein dispersibility index of at least 95.0%and wherein a 1.0% solution (w/w) in water of the protein hydrolyzatehas a visible light transmittance of least 90.0%. In a furtherembodiment, the oilseed protein hydrolyzate has a protein dispersibilityindex of at least 99.0%. In an embodiment, the oilseed proteinhydrolyzate has a protein dispersibility index of at least 99.8%.

In another embodiment of the disclosure, a 1.0% solution (w/w) of theprotein hydrolyzate has a visible light transmittance of least 95.0%. Ina further embodiment, a 1.0% solution (w/w) of the protein hydrolyzatehas a visible light transmittance of least 97.0%. In another embodiment,a protein hydrolyzate produced in accordance with a process of thepresent disclosure contains less than about 1% (w/w) fiber, optionallyless than about 0.5% (w/w) fiber, and optionally less than about 0.1%(w/w) fiber.

In another embodiment of the disclosure, there is also included anoilseed protein concentrate having a protein content of about 60% toabout 90%, wherein the protein has a methionine content at least 1.90%by weight and a cysteine content at least 1.60% by weight. In anembodiment, the oilseed protein concentrate has a methionine content atleast 1.95% by weight. In an embodiment, the oilseed protein concentratehas a methionine content at least 2.02% by weight. In an embodiment, theoilseed protein concentrate has a cysteine content at least 1.65% byweight. In an embodiment, the oilseed protein concentrate has a cysteinecontent at least 1.68% % by weight.

In another embodiment of the disclosure, a protein concentrate producedin accordance with a process of the present disclosure, contains lessthan about 5% (w/w) of fiber, optionally about 0.5% to about 5% (w/w).

In an embodiment, the protein concentrate possessing a protein contentof about 60% to about 70% produced in accordance with the processes ofthe present disclosure are utilized as a protein ingredient in aquafeedsfor fish, swine and pet foods.

In another embodiment, the protein concentrate possessing a proteincontent of about 70% to about 75% produced in accordance with theprocesses of the present disclosure are useful as a protein ingredientfor baked food products such as bread, rolls, cake and pastry products(including mixtures for preparing baked food products), cookies,biscuits, crackers, pancakes, pastries, doughnuts, and other pastaproducts. In addition, this protein concentrate is useful as a proteiningredient in meat products such as baked meat, hot dogs, bologna,analogs, ham and sausages. Further, this protein concentrate is alsouseful as a protein ingredient in vegetarian foods. It will beunderstood by a person skilled in the art that this protein concentrateis also useful for other applications where a lower grade of proteinconcentrate is sufficient, such as in aquafeeds and pet foods asdescribed above.

In another embodiment, the protein concentrate possessing a proteincontent of about 75% to less than 90% produced in accordance with theprocesses of the present disclosure is useful as a protein ingredient inbreakfast cereals, and baked goods, as well as meat products such asbologna, frankfurters, luncheon loaves and ham. Further, this proteinconcentrate is useful in candies, confections, desserts, dietary items,Asian foods, soup mixes, gravies and other similar food items. Again, itwill be understood by a person skilled in the art that this proteinconcentrate is also useful for other applications where a lower grade ofprotein concentrate is sufficient, such as in aquafeeds, pet foods,bakery products and meat products, as described above.

In another embodiment, the protein isolate possessing a protein contentof greater than 90% produced in accordance with the processes of thepresent disclosure is useful as a protein ingredient in nutritionalbeverages such as protein fortified soft drinks, sports drinks, fruitjuices and other high protein drinks. In addition, this protein isolateis useful as a protein ingredient for nutritional supplements, specialdiet products, and high protein nutritional tablets. In addition, theprotein isolate is useful as a protein ingredient in infant formulas, aswell as an ingredient in comminuted and emulsified meats, simulatedmeats, combination meat products and cured or uncured meat products.Further, the protein isolate is useful as a protein ingredient in pasta(e.g. macaroni), bread and other bakery products, pancakes, waffles,crackers, donuts, pie crusts, soups, egg replacements, dried milkreplacements and dairy analogs. Again, it will be understood by a personskilled in the art that this protein isolate is also useful for otherapplications where a lower grade of protein is sufficient, such as inaquafeeds, pet foods, and meat products, as described above.

In another embodiment, the hydrolyzed protein isolate possessing aprotein content of greater than 90% produced in accordance with theprocesses of the present disclosure is useful as a protein ingredient innutritional beverages such as protein fortified soft drinks, sportsdrinks, fruit juices and other high protein drinks. In addition, thehydrolyzed protein isolate is useful as a cosmetic ingredient. Further,the hydrolyzed protein isolate is useful as a protein ingredient forhealthy food applications to improve absorption and digestibility.Again, it will be understood by a person skilled in the art that thishydrolyzed protein isolate is also useful for other applications where alower grade of protein is sufficient, such as in aquafeeds, pet foods,bakery products and meat products, as described above.

In another embodiment, there is also included a protein concentratehaving a protein content of at least 60% and less than 90% proteincomprising:

i) a first protein fraction comprising between 30% and 70% 2S protein,optionally between 40% and 60%, optionally 45% and 55%;

ii) a second protein fraction comprising between 20% and 50% 12Sprotein, optionally between 25% and 45%, optionally between 30% and 40%,optionally between 35% and 40%.

In another embodiment, there is also included a protein isolate having aprotein content of at least 90% protein comprising:

i) a first protein fraction comprising between 10% and 40% 2S protein,optionally between 15% and 30%;

ii) a second protein fraction comprising between 30% and 70% 12Sprotein, optionally 40% and 60%, optionally between 50% and 60%.

(III) Processes of the Disclosure

A person skilled in the art would be able to produce a protein-enrichedmeal using methods that are well known in the art. A general method forobtaining a protein-enriched meal is shown in FIGS. 1 and 2. Forexample, when beginning with an oilseed, such as canola, rapeseed,mustard seed, broccoli seed, flax seed, cotton seed, hemp seed,safflower seed, sesame seed or soybean meal, in particular canola, themoisture content of the oilseed is adjusted. The moisture adjustedoilseed is optionally exposed to a heat treatment. In an embodiment ofthe processes of the present disclosure, the oilseed is heat treated toa temperature of about 60° C. to about 120° C., optionally about 70° C.to about 100° C., or about 80° C. to about 90° C., or about 80° C. Inanother embodiment, the heat treatment is carried out at a temperatureof 100° C. The heat treatment of the oilseed results in the inactivationof the enzymes present in the oilseed, for example, myrosinase, lipase,phospholipase. If the oilseed is not heat treated, the enzymes (such asmyrosinase, lipase, phospholipase), as a result of their enzymaticaction, can degrade the oil and breakdown glucosinolates releasingsulphur into oil. However, a heat treatment can also denature theproteins in the concentrate or isolate. At a temperature of about75-100° C., the enzymes are deactivated, and are therefore not able todegrade the oil and breakdown glucosinolates releasing sulphur into oil,while the protein within the oilseed is not denatured. The selection ofa heat treatment temperature is a compromise between the opposingeffects on oil quality, meal quality and economics. Accordingly, in anembodiment, a heat treatment temperature of 75-100° C. results in areasonably high protein dispersibility index (PDI), lower sulphur, FFAand phosphorus in pressed and butane/R134a extracted oils.

Alternatively, in an embodiment, the oilseed is not exposed to a heattreatment and its moisture content is not adjusted. It will beunderstood by a person skilled in the art that the moisture content ofthe seed is typically in the range of about 7% to about 10% for apressing operation. If the moisture content of the seed is not in thisrange, the moisture of the seed is optionally adjusted to about 7% toabout 10% by adding water or drying, which is followed by blending andtempering.

The oilseed is then pressed to remove the oil from within the oilseed.Generally, an oilseed such as canola, rapeseed, mustard seed, broccoliseed, flax seed, cotton seed, hemp seed, safflower seed, sesame seed orsoybean, contains about 15% to about 50% oil (w/w), depending on theparticular oilseed. Typically, oil is removed from an oilseed bypressing the oil from the oilseed to form a pressed oilseed. Examples ofpressed oilseeds are a seedcake (or a presscake), while a defatted mealor a protein-enriched meal begin from a seedcake (or presscake), asexplained below. It will be understood that a seedcake and a presscakedefine the same pressed seed meal. Methods of pressing oil from anoilseed are well known in the art. A typical pressing will remove about30% to about 70% of the oil in the oilseed, and results in pressed oiland a pressed seedcake (or presscake).

In an embodiment, the removal of much of the remaining oil from theseedcake is accomplished by solvent extraction of the seedcake. Solventextraction is a well known process in the art and utilizes low boilingsolvents, such as hexane, methyl pentane or other refrigerants such asITFM and R134a (1,1,1,2-tetrafluoroethane), to remove residual oil fromthe seedcake.

The solvent extraction process results in a defatted seedcake meal and asolution of solvent and oil. The oil is separated from the solvent andutilized for other purposes. Generally, depending on the extractionprocess, the seedcake will contain residual amounts of solvent that areremoved from the seedcake. Typically, the removal of the residualsolvent from seedcake is accomplished by heating the seedcake in adesolventizer toaster (DT), flash desolventizer (such as a ring dryer)or vacuum oven, which causes the residual solvent to evaporate. Theseedcake is subsequently dried. The above process removes much of theoil from the pressed oilseed and leaves material known as defatted meal.In an embodiment, the defatted meal will contain less than about 6% ofoil, optionally about 0.5% to about 3% (w/w).

The defatted meal is then subjected to a milling step and a screeningstep to obtain a pressed oilseed known as a protein-enriched meal.

The defatted meal is typically milled, for example with a disc mill or ahammer mill, to reduce the particle size of the defatted meal. Whenusing a disc mill, the defatted meal is forced through two rotatingdiscs which crush the defatted meal. When a hammer mill is used toreduce the particle size of the defatted meal, the meal is loaded intothe hammer mill, wherein the hammers reduce the particle size of thedefatted meal.

After the particle size of the defatted meal has been sufficientlyreduced, the milled defatted meal is screened through mesh screens,which results in an initial separation of a fiber fraction from thedefatted meal, resulting in a protein-enriched meal. Fiber tends to havea larger particle size which is not able to pass through the screen.However, a portion of the fiber will be able to pass through the screen,and as such, only a portion of the fiber is removed by screening.Typically, about a 45 US mesh screen is used for the initial fiberseparation. This is a dry screening process which results in a fiberenriched meal, which does not pass through the screen, and theprotein-enriched meal, which does pass through the screen. Theprotein-enriched meal, however, still contains a significant amount offiber and other antinutritional factors. From the milled defattedmaterial, about a 30% to about 60% by weight protein-enriched meal istypically obtained, while the fiber fraction constitutes about 40% toabout 70% of the original weight of the defatted material. Theprotein-enriched meal possesses a protein content of about 40% to about60%, optionally 50% to about 55%, while the fiber fraction possessesabout 35% to about 48% protein content. In an embodiment of thedisclosure, it is this protein-enriched meal that is utilized to producethe protein concentrates and protein isolates of the present disclosure.However, in another embodiment, it will be apparent to those skilled inthe art that a seedcake, defatted meal or protein-enriched meal isutilized with the processes of the present disclosure. The use of such adefatted or protein-enriched meal, and processing with a minimum amountof heat during conditioning, pressing, solvent extraction,desolventization and drying, leads to better protein concentrates andprotein isolates.

In an embodiment of the present disclosure, there is a process forremoving fiber from a partially defatted, fully defatted orprotein-enriched meal or “meal”). In particular, the process relates toseparating and removing fiber from a meal based on the density andparticle size differences between the fiber particles and the proteinparticles. The separation and removal of fiber is accomplished by usingseparation methods, at specific speeds, which can separate particlesbased on their density or particle size such as centrifugation, gravitysedimentation, a gravity table or hydrocyclone to separate the fiberfrom the mixture and form the protein slurry. In an embodiment, theseparation is accomplished using centrifugation. In another embodiment,the separation is accomplished using a decanter centrifuge. In anotherembodiment, the separation is accomplished using a decanter centrifugeat a speed of about 1,000 rpm to about 2,000 rpm. In another embodiment,the separation is accomplished using a decanter centrifuge at a speed ofabout 1,500 rpm. In an embodiment, the centrifugation of a meal mixtureresults in three layers: i) an insoluble fiber layer and a proteinslurry on top of the fiber, which is comprised of ii) an insolubleprotein fraction and iii) a soluble protein fraction. Separation of thetop and middle layers (the soluble protein extract and the insolublefine protein fraction) from the bottom layer (coarse fiber solids),results in a protein slurry with fiber removed.

In an embodiment of the present disclosure, a process for the productionof a protein concentrate possessing a protein content of about 60% toabout 70% is obtained from a defatted or protein-enriched meal. Anoptional general process for the production of a protein concentrate isillustrated in FIG. 3.

In an embodiment, a defatted or protein-enriched meal is produced by theprocess above, and is then washed at least once with about 5% to about100%, optionally about 20% to about 90%, or about 40% to about 80% (v/v)ethanol in water, resulting in an ethanol extract and an ethanol washeddefatted or protein-enriched meal. Other alcohols, such as methanol orisopropanol, can be utilized for washing the defatted orprotein-enriched meal. In an embodiment, ethanol is used for washing thedefatted or protein-enriched meal because it is less toxic than otheralcohols, and a higher percentage of ethanol residue is allowed in thefinal product.

In another embodiment, the defatted or protein-enriched meal is washedonce with ethanol, wherein the ratio of ethanol to the protein-enrichedmeal is about 1:3 to about 1:15, typically about 1:4 to about 1:8,optionally 1:6, on a weight-to-weight basis of protein-enriched meal toethanol.

In another embodiment, the defatted or protein-enriched meal is washedtwice with ethanol, wherein the amount of ethanol added to theprotein-enriched meal results in a ratio of about 1:2 to about 1:15,typically about 1:5 to about 1:8, optionally 1:6, on a weight-to-weightbasis of protein-enriched meal to ethanol. Typically, washing thedefatted or protein-enriched meal at least twice results in the removalof more impurities from the defatted or protein-enriched meal andtherefore increases the protein content in the protein concentrate.

In a further embodiment, the defatted or protein-enriched meal is washedin a counter-current extractor. In this embodiment, the defatted orprotein-enriched meal is washed about 2 times to about 10 times, whereinthe ratio of solvent to the defatted or protein-enriched meal is about 1to about 10 of meal to about 1 of meal.

In another embodiment, the defatted or protein-enriched meal is washedwith ethanol at a temperature of about 10° C. to about 90° C.,optionally 20° C. to about 60° C., suitably at a temperature of about40° C. to about 60° C.

The ethanol extract is optionally separated from the ethanol washeddefatted or protein-enriched meal by centrifugation, filtration, vacuumfiltration, pressure filtration, sedimentation, decantation or gravitydraining. With respect to centrifugation, the ethanol mixture istypically fed to a decanter centrifuge or a basket centrifuge. Theethanol extract is then separated from the ethanol washed defatted orprotein-enriched meal by centrifugal force. For the decanter centrifuge,a screw conveyer is contained within a solid bowl and both rotate athigh speeds. Solids settling on the bowl are conveyed by the screwconveyer out of the centrifuge. For a basket centrifuge, which consistsof a perforated basket rotating inside a stationary housing, the ethanolmixture is fed into the basket and centrifugal force pushes it againstthe filter liner. The solids are retained by the liner while the liquidpasses through. For filtration, the ethanol extract is typicallyseparated from the ethanol washed defatted or protein-enriched meal bydraining through a perforated belt or basket in a reactor. For vacuumfiltering or pressure filtering, the separation is aided by vacuum orpressure. In an embodiment, the ethanol extract is concentrated byevaporation of the ethanol to form a high sugar fraction, optionallycontaining antinutritional factors that can be further purified. Theantinutritional compounds may be purified into valuable pharmaceutical,medicinal or chemical compounds, such as glucosinolates, phytic acid orphytates, sinapine and sinigrin. In an embodiment, the ethanol extractis heated under vacuum at about 30° C. to about 90° C., which results inthe evaporation of ethanol and water, and soluble solids are leftbehind. Ethanol is further separated from water by distillation andre-used in the process. The concentrated high-sugar fraction is dried byspray drying, rotary drum drying, vacuum drying, flash drying, ringdrying, microwave drying, freeze drying or using a fluidized bed dryer.

In another embodiment, the washed defatted or protein-enriched meal isdried to form the protein concentrate, possessing a protein content ofabout 60% to about 70%. In a further embodiment, the washedprotein-enriched meal is dried in a spray dryer, drum dryer, vacuumdryer, fluidized bed dryer or ring dryer to form the protein concentratepossessing a protein content of about 60% to about 70%. These dryersremove the solvent by drying the protein concentrate under a vacuum orat atmospheric pressure at elevated temperatures of about 30° C. toabout 100° C.

In an embodiment, the protein concentrate is dried to a moisture contentof about 1% to about 10%, optionally about 4% to about 8%.

In another embodiment, the ethanol that is removed through drying isrecovered and recycled so it can be used again in further ethanolextractions. The ethanol is recovered through evaporation anddistillation.

In another embodiment, the dried protein concentrate possessing aprotein content of about 60% to about 70% is further milled into powderform without coarse particles.

In another embodiment of the present disclosure, there is provided aprocess for producing a protein concentrate possessing a protein contentof about 70% to about 75% on a dry weight basis. In an embodiment, ageneral process for the production of a protein concentrate possessing aprotein content of about 70% to about 75% is illustrated in FIGS. 4-7,where the removal of fiber is also detailed. In an embodiment, the useof an extraction solvent, such as ethanol, leads to a proteinconcentrate or protein isolate having superior organoleptic properties,as well as superior water solubility properties, which thereforepossesses better functional properties.

Accordingly, in an embodiment of the present disclosure, a process forthe production of a protein concentrate from a defatted orprotein-enriched meal is disclosed, comprising:

-   -   1) removing fiber from the defatted or protein-enriched meal,        comprising either:        -   i) mixing the defatted or protein-enriched meal with a            mixing solvent to form a first mixture;            -   screening the first mixture through a mesh screen of                about 10 to about 200 US mesh size to remove the fiber;                or        -   ii) mixing the defatted or protein-enriched meal with water            to form a second mixture;            -   optionally adjusting the pH of the second mixture to a                pH of about 3 to about 7; and            -   adding cellulase complex to the second mixture and                heating to a temperature of about 30° C. to about 60° C.                to hydrolyze the fiber;    -   2) washing the first or second mixture with an extraction        solvent to form an extract and a washed defatted or        protein-enriched meal;    -   3) separating the extract from the washed defatted or        protein-enriched meal;    -   4) optionally repeating steps 2) and 3) at least one more time;        and    -   5) desolventizing the washed defatted or protein-enriched meal        to form a protein concentrate.

In an embodiment of the present disclosure, the mixing solvent is anysolvent which forms a slurry with the defatted or protein-enriched mealwhen mixed together and is able to suspend the protein within themixture. In another embodiment, the mixing solvent comprises water,methanol, ethanol, or isopropanol, or mixtures thereof. In a furtherembodiment, the mixing solvent comprises water or ethanol, and mixturesthereof.

In another embodiment, the defatted or protein-enriched meal comprises acanola, rapeseed, mustard seed, broccoli seed, flax seed, cotton seed,hemp seed, safflower seed, sesame seed or soybean meal. In a furtherembodiment, the protein-enriched meal comprises a canola meal, a soybeanmeal, a mustard seed meal or a flax seed meal.

In an embodiment of the disclosure, the defatted or protein-enrichedmeal is mixed with a mixing solvent in a ratio of about 3 to about 10parts solvent to about 1 part of the defatted or protein-enriched meal,on a weight-to-weight basis.

In an embodiment of the present disclosure, the pH of the first mixtureis adjusted to a pH of about 3.0 to about 10.0, optionally about 6.8 toabout 7.2 with a solution of an alkali metal base or an acid, such asphosphoric, hydrochloric or sulphuric acid. In a further embodiment, asolution of an alkali metal base comprising about 1% to about 40% byweight, optionally about 5% to about 30%, of the alkali metal base andwater is added to the first mixture. In another embodiment, the alkalimetal base comprises sodium hydroxide (NaOH).

In another embodiment of the present disclosure, the first mixture isthoroughly agitated. In another embodiment, an inline mixer is used forthorough mixing of the first mixture. Thorough mixing of the firstmixture disperses the protein particles and releases natural sugarcompounds that are trapped inside the insoluble protein particles in themixing solvent. In addition, the agitation suspends the solids of theprotein-enriched meal in the mixing solvent.

In a further embodiment, the thoroughly mixed first mixture is wetscreened resulting in a separation of the fiber from the mixture whichcontains the protein. In another embodiment of the disclosure, the meshscreen comprises a US mesh screen of about 20 to about 200 US mesh. In afurther embodiment, the mesh screen is a vibratory screen. A personskilled in the art would recognize that other screens, for examplerevolving screens, shaking screens or oscillating screens, could be usedin place of vibratory screens to perform substantially the same functionof vibrating the mixture which aids in separation of the first mixturefrom the fiber. In an embodiment of the disclosure, the fiber in themeal swells upon addition of the mixing solvent, increasing the particlesize of the fiber. Consequently, the mesh screen prevents the fiber frompassing through, while the protein in the first mixture passes throughthe screen, resulting in a separation of the fiber from the protein. Inan embodiment, the fiber fraction is dried and can be used in dietaryfiber products. The fiber fraction optionally contains protein andcarbohydrates.

In another embodiment of the present disclosure, the defatted orprotein-enriched meal is thoroughly mixed with water to form the secondmixture. In an embodiment, wet milling is used to mix the secondmixture. In another embodiment, an inline mixer is used to thoroughlymix the second mixture. In an embodiment, the mixing of the defatted orprotein-enriched meal in water, results in the internal fiber structurebeing exposed, which allows for the cellulase complex to efficientlyhydrolyze the fiber.

In a further embodiment of the disclosure, the pH of the second mixtureis optionally adjusted with an acid. In an embodiment, the pH of thesecond mixture is adjusted to a pH that is suitable for the activity ofan enzyme within the second mixture. In an embodiment, the pH of thesecond mixture is adjusted to a pH of about 3 to about 7. The pH of thesecond solution is adjusted with an acid solution. In an embodiment, theacid solution is phosphoric acid, hydrochloric acid or sulfuric acid. Inan embodiment, the natural pH of the second mixture is about 6.8 toabout 7.2, and therefore the pH of the second mixture is not adjusted.

In another embodiment of the present disclosure, the cellulase complexis added to the second mixture in an amount of about 1 to about 10 grams(about 0.1% to about 1%) to about 1 kg of dried solids in the secondmixture. In a further disclosure, the cellulase complex is mixed withthe second mixture for about 0.5 hours to about 5 hours. In anotherembodiment, the cellulase complex is mixed with the second mixture forabout 1 to about 3 hours. It will be apparent to those skilled in theart that cellulase complex contains different types of cellulase enzyme.For example, cellulase complex contains at least one of endocellulase,exocellulase, cellobiohydrolase, cellobiase, endohemicellulase andexohemicellulase. Cellulase enzymes possess enzymatic activity which areable to hydrolyze the fiber to constituent sugars within the secondmixture.

In another embodiment of the present disclosure, the first or secondmixture is washed at least once with about 5% to about 100%, optionallyabout 25% to about 85%, or about 50% to about 85%, or about 60% to about85%, of the extraction solvent (v/v) in water. The addition of theextraction solvent precipitates proteins in the first or second mixture,while the carbohydrates from the oilseed and from the hydrolyzation ofthe fiber remain in the extraction solvent, which allows for separation.It will be understood that an extraction solvent will be any solventwhich dissolves the carbohydrates and other undesirable compounds, butprecipitates the protein. In embodiment, the extraction solvent iswater, methanol, ethanol or isopropanol, and mixtures thereof. Inanother embodiment, the extraction solvent is ethanol. It will beunderstood by a person skilled in the art that if the extraction solventcomprises 100% extraction solvent, no water will be present in theextraction solvent. For example, the extraction solvent could be 100%ethanol. In another embodiment, the extraction solvent is 60% ethanol inwater.

In an embodiment of the present disclosure, the extraction solvent isadded in an amount to adjust the ratio of the extraction solvent to thefirst or second mixture of about 5% to about 95%, optionally about 10%to about 90%, or about 40% to about 80% (v/v) of the extraction solvent.

In an embodiment of the present disclosure, the first or second mixtureis washed with an extraction solvent at a temperature of about 10° C. toabout 90° C.

In another embodiment, the first or second mixture is washed with theextraction solvent at a temperature of about 20° C. to about 60° C. In afurther embodiment, the first or second mixture is washed with theextraction solvent at a temperature of about 20° C. to about 25° C.

In another embodiment of the present disclosure, the extract isseparated from the washed defatted or protein-enriched meal bycentrifugation, vacuum filtration, pressure filtration, decantation orgravity draining. In an embodiment, the extract is concentrated byevaporation of the extraction solvent dried to form a high sugarfraction, as is performed above.

In another embodiment of the disclosure, steps 2) and 3) are optionallyrepeated at least once. In an embodiment, steps 2) and 3) are repeatedat least twice. Repeating steps 2) and 3) results in a protein productcontaining less impurities, such as fiber and other antinutritionalfactors.

In another embodiment, the washed defatted or protein-enriched meal isdried to form the protein concentrate, possessing a protein content ofabout 70% to about 75% on a dry weight basis. In a further embodiment,the washed defatted or protein-enriched meal is dried in a vacuum dryer,fluidized bed dryer, spray dryer or ring dryer to form the proteinconcentrate possessing a protein content of about 70% to about 75%.

In another embodiment, the washed defatted or protein-enriched meal isdried to a moisture content of about 0.5% to about 12%, optionally about1% to about 10%, or about 4% to about 8%. In a further embodiment, thewashed defatted or protein-enriched meal is dried to a moisture contentof about 6%.

In another embodiment of the disclosure, the extraction solvent that isremoved through drying is recovered and recycled so it can be used againin further extractions.

In another embodiment, the dried protein concentrate possessing aprotein content of about 70% to about 75% is further milled into powderform.

In another embodiment of the present disclosure, there is disclosed aprocess for the production of a protein concentrate comprising a proteincontent of about 75% to less than 90% on a dry weight basis. In anembodiment, a general process for the production of a proteinconcentrate possessing a protein content of about 80% and a proteinisolate having a protein content greater than 90% is illustrated inFIGS. 8-9.

Accordingly, a process for the production of a protein concentrate froma defatted or protein-enriched meal is disclosed, comprising:

removing fiber from the defatted or protein-enriched meal, comprising:

-   -   i) mixing the defatted or protein-enriched meal with a mixing        solvent to form a mixture;        -   optionally screening the mixture through a mesh screen of            about 10 to about 200 US mesh size to remove fiber,        -   optionally adjusting the pH of the mixture to a pH of about            7;        -   optionally milling the mixture;        -   centrifuging the mixture to remove fiber,    -    and forming a protein slurry; and    -   ii) centrifuging the protein slurry to form a protein        precipitate and a soluble protein fraction;    -   iii) washing the protein precipitate with an extraction solvent        at least once and centrifuging to form a purified protein        precipitate;    -   iv) drying the purified protein precipitate to form the protein        concentrate.

It will be understood by a person skilled in the art that the steps ofthe process do not have to be followed exactly. For example, a personskilled in the art would recognize that the milling step could beperformed before the screening step.

In another embodiment, the defatted or protein-enriched meal comprises acanola, rapeseed, mustard seed, broccoli seed, flax seed, cotton seed,hemp seed, safflower seed, sesame seed or soybean meal. In a furtherembodiment, the protein-enriched meal comprises a canola meal. In anembodiment, the protein-enriched meal comprises a soybean meal. Inanother embodiment, the protein-enriched meal comprises mustard seedmeal. In a further embodiment, the protein-enriched meal comprises flaxseed meal.

In an embodiment of the disclosure, the mixing solvent is any solventwhich forms a slurry with the defatted or protein-enriched meal and isable to suspend the protein within the mixture. In another embodiment,the mixing solvent comprises water, methanol, ethanol, or isopropanol,and mixtures thereof. In a further embodiment, the solvent compriseswater or ethanol, and mixtures thereof.

In an embodiment, the defatted or protein-enriched meal is mixed withthe mixing solvent to form a mixture in a ratio of defatted orprotein-enriched meal to mixing solvent of about 1:3 to about 1:20,optionally about 1:6 to about 1:10, or about 1:6 to about 1:8.

In a further embodiment, the mixture is wet screened resulting in aseparation of the fiber from the mixture which contains the protein. Inanother embodiment of the disclosure, the mesh screen comprises a USscreen of size about 20 to about 200 mesh. In a further embodiment, themesh size is 40 US mesh size. In a further embodiment, the mesh screenis a vibratory screen. The mesh screen prevents the fiber from passingthrough, while the protein in the mixture passes through the screen,resulting in a separation of the fiber from the protein. In anembodiment, the fiber fraction is dried and can be used in dietary fiberproducts. In an embodiment, protein and carbohydrates are present in thefiber fraction.

In another embodiment, the pH of the mixture is adjusted to about 7 withthe addition of aqueous sodium hydroxide. In a further embodiment, theaqueous sodium hydroxide is a solution of about 1% to about 40%,optionally about 5% to about 30%, by weight of sodium hydroxide inwater.

In another embodiment, the mixture is optionally milled using a wetmilling process. In an embodiment, the wet milling of the mixtureresults in thorough mixing of the defatted or protein-enriched meal withthe mixing solvent. Thorough mixing of the mixture disperses the proteinparticles and releases natural sugar compounds that are trapped insidethe insoluble protein particles in the mixing solvent. In addition, themixing suspends the solids of the protein-enriched meal in the mixingsolvent.

In another embodiment of the present disclosure, the mixture iscentrifuged using a decanting centrifuge. In an embodiment, the mixtureis centrifuged with a decanting centrifuge at a speed of about 1000 rpmto about 2000 rpm. In another embodiment, the speed is about 1500 rpm.

In another embodiment, the protein slurry is then centrifuged using adisc stack centrifuge to separate insoluble proteins from solubleproteins, forming a protein precipitate and a soluble protein fraction.In an embodiment, the protein slurry is pumped to a disc centrifuge. Thecentrifuge has a bowl which spins at about 7500 rpm. As the slurryenters the centrifuge bowl, the slurry is brought up to the same speedas the bowl, which results in high centrifugal forces, about 6500 timesthe force of gravity acting on the mixture. The heavier proteinprecipitate is forced to the outside of the bowl. The soluble proteinfraction is forced towards the axis of the bowl. The heavy precipitatecollects around the outside of the bowl which are removed from the bowlperiodically or continuously. The protein slurry is fed to thecentrifuge continuously while the liquid soluble protein fraction ispumped out continuously. In an embodiment, the disc centrifuge operatesat a speed of about 6500 rpm to about 8500 rpm.

In a further embodiment, the protein precipitate is washed with anextraction solvent to purify the protein precipitate and dissolveresidual sugars and other non-desirable compounds. It will be understoodthat an extraction solvent will be any solvent which dissolves thecarbohydrates and other non-desirable compounds. In an embodiment, theextraction solvent is water, methanol, ethanol or isopropanol, andmixtures thereof. In another embodiment, the extraction solvent is wateror ethanol, and mixtures thereof. In another embodiment, the extractionsolvent is water. In an embodiment, the protein precipitate is washed atleast twice with the extraction solvent.

In another embodiment, the washed protein precipitate is thencentrifuged again with a disc stack centrifuge at a speed of about 6500rpm to about 8500 rpm to obtain a protein precipitate. In anotherembodiment, the washing extracts from the centrifugation are added tothe soluble protein fraction.

In another embodiment, the washed protein precipitate is dried to form aprotein concentrate comprising a protein content of about 75% to about90% on a dry weight basis. In a further embodiment, the washed proteinprecipitate is dried in a vacuum dryer, fluidized bed dryer or ringdryer to form the protein concentrate possessing a protein content ofabout 75% to less than 90%. It will be understood by a person skilled inthe art that the washed protein precipitate can be used as a proteinisolate without drying. However, the dried protein isolate has a bettershelf life as removal of the solvent, for example water, results in amore stable protein isolate.

In another embodiment of the present disclosure, there is provided aprocess for the production of a protein isolate comprising a proteincontent of greater than 90% on a dry weight basis. In an embodiment, ageneral process for the production of a protein isolate and hydrolyzedproteins having a protein content greater than 90% is illustrated inFIGS. 10-11.

Accordingly, a process for the production of a protein isolate from adefatted or protein-enriched meal is disclosed, comprising:

removing fiber from the defatted or protein-enriched meal, comprising:

-   -   i) mixing the defatted or protein-enriched meal with a mixing        solvent to form a mixture;        -   screening the mixture through a mesh screen of about 10 to            about 200 US mesh size to remove fiber,        -   optionally adjusting the pH of the mixture to a pH of about            7;        -   optionally milling the mixture; and        -   centrifuging the mixture to remove fiber,    -    and forming a protein slurry;    -   ii) centrifuging the protein slurry to form a protein        precipitate and a soluble protein fraction;    -   iii) filtering the soluble protein fraction; and    -   iv) drying the soluble protein to form the protein isolate.

In an embodiment, the soluble protein fraction is obtained using thesame process as described above.

It will be understood by a person skilled in the art that the steps ofthe process do not have to be followed exactly. For example, a personskilled in the art would recognize that the milling step could beperformed before the screening step.

In another embodiment, the defatted or protein-enriched meal comprises acanola, rapeseed, mustard seed, broccoli seed, flax seed or soybeanmeal. In a further embodiment, the protein-enriched meal comprises acanola meal. In an embodiment, the protein-enriched meal comprises asoybean meal. In another embodiment, the protein-enriched meal comprisesmustard seed meal. In a further embodiment, the protein-enriched mealcomprises flax seed meal.

In an embodiment of the disclosure, the mixing solvent comprises wateror a salt solution. In an embodiment, the salt solution comprises lessthan 5%, optionally about 3% to about 4%, or 3.5% by weight of salt insolution. In a further embodiment, the mixing solvent comprises water.In another embodiment, the ratio of defatted or protein-enriched meal tothe mixing solvent is about 1:3 to about 1:20. In a further embodiment,the ratio is about 1:6 to about 1:10. In an embodiment, the ratio isabout 1:6 to about 1:8.

In an embodiment, the soluble protein fraction is purified byultrafiltration and diafiltration using a membrane filtration apparatus.In an embodiment, when ultrafiltration is utilized, the soluble proteinfraction is heated to a temperature of about 1° C. to about 60° C.,optionally 40° C. to about 55° C., before being passed through anultrafiltration apparatus fitted with membranes to filter proteinslarger than about 10,000 daltons, optionally about 30,000, or about100,000 daltons. The filtered protein is recycled back to the feed tankwhile the liquid is discarded. The ultrafiltration process is continueduntil the amount of protein that has been filtered in the feed tank isequal to about 30% to about 40% of its initial weight of the solubleprotein fraction.

In a further embodiment, when diafiltration is utilized, it is conductedat about 1° C. to about 60° C., optionally about 40° C. to about 55° C.,using the diafiltration unit, which is fitted with the membranes tofilter proteins larger than about 10,000 daltons, optionally about30,000, or about 100,000 daltons. The original volume of soluble proteinfraction in the feed tank is held constant by adding water to make upfor the removed liquid. The filtered protein is recycled back to thefeed tank. The amount of water added to maintain the original volume ofprotein solution is about 2 times the original volume of soluble proteinfraction. For example, if 100 L of soluble protein fraction is used, 200L of water is added to the soluble protein fraction in the feed tankduring the cycle of diafiltration. The volume of the feed tank is keptconstant at 100 L with the continued addition of water to the feed tankwhile the liquid is removed from the system through diafiltration.

In an embodiment, after the soluble protein fraction has been filtered,the filtered soluble protein is spray dried to form a high functionalprotein isolate comprising a protein content of greater than about 90%on a dry weight basis. It will be understood by a person skilled in theart that spray drying is the transformation of a feed from a fluid stateinto a dried form by spraying the feed into a circulating hot airmedium. Generally, spray drying transforms the filtered protein intomany droplets which are then exposed to a fast current of hot air. As aresult of the very large surface area of the droplets the water in theprotein evaporates almost instantaneously and the droplets aretransformed into powdery dry protein particles. In an embodiment, theinlet temperature is about 180° C. to about 220° C. which is thetemperature of the hot air entering the spray dryer chamber, the outlettemperature is about 75° C. to about 90° C., which is the temperature ofthe exhaust, and the feed temperature is about 40° C. to about 50° C. Itwill be understood by a person skilled in the art that the washedprotein precipitate can be used as a protein isolate without drying.However, the dried protein isolate has a better shelf life as removal ofthe solvent, for example water, results in a more stable proteinisolate.

In another embodiment of the present disclosure, there is provided aprocess for the production of a protein isolate which is subsequentlymodified or hydrolyzed to form a high functional protein isolate or amixture of hydrolyzed proteins, peptides and amino acids comprising aprotein content of greater than 90% on a dry weight basis.

Accordingly, in an embodiment of the present disclosure, a process forthe production of a protein isolate from a defatted or protein-enrichedmeal is disclosed, comprising:

removing fiber from the defatted or protein-enriched meal, comprising:

-   -   i) mixing the defatted or protein-enriched meal with a mixing        solvent to form a mixture;        -   optionally screening the mixture through a mesh screen of            about 10 to about 200 US mesh size to remove fiber,        -   optionally adjusting the pH of the mixture to a pH of about            7;        -   optionally milling the mixture; and        -   centrifuging the mixture to remove fiber,    -    and forming a protein slurry;    -   ii) centrifuging the protein slurry to form a protein        precipitate and a soluble protein fraction;    -   iii) mixing the protein precipitate with water to form a protein        precipitate mixture and optionally adjusting the pH of the        mixture to a pH of about 3 to about 7;    -   iv) adding cellulase complex to the protein precipitate mixture        to hydrolyze residual fiber;    -   v) washing the protein precipitate with an extraction solvent        and centrifuging to form a protein isolate.

It will be understood by a person skilled in the art that the steps ofthe process do not have to be followed exactly. For example, a personskilled in the art would recognize that the milling step could beperformed before the screening step.

In another embodiment, the defatted or protein-enriched meal comprises acanola, rapeseed, mustard seed, broccoli seed, flax seed or soybeanmeal. In a further embodiment, the protein-enriched meal comprises acanola meal. In an embodiment, the protein-enriched meal comprises asoybean meal. In another embodiment, the protein-enriched meal comprisesmustard seed meal. In a further embodiment, the protein-enriched mealcomprises flax seed meal.

In another embodiment of the disclosure, the mixing solvent compriseswater or a salt solution. In an embodiment, the salt solution comprisesless than 5%, optionally about 3% to about 4%, or 3.5% by weight of saltin solution. In a further embodiment, the mixing solvent compriseswater. In another embodiment, the ratio of defatted or protein-enrichedmeal to the mixing solvent is about 1:3 to about 1:20. In a furtherembodiment, the ratio is about 1:6 to about 1:10. In an embodiment, theratio is about 1:6 to about 1:8.

In a further embodiment, the mixture is wet screened resulting in aseparation of the fiber from the mixture which contains the protein. Inanother embodiment of the disclosure, the mesh screen comprises a USmesh screen of size about 20 to about 200 mesh. In an embodiment, themesh screen is of size 40 US mesh size. In a further embodiment, themesh screen is a vibratory screen. The mesh screen prevents the fiberfrom passing through, while the protein in the mixture passes throughthe screen, resulting in a separation of the fiber from the protein.This results in a mixture of protein which passes through the screen anda fiber fraction which is trapped by the screen. In an embodiment, thefiber fraction is dried and can be used in dietary fiber products.

In an embodiment, some protein and carbohydrates are present in thefiber fraction.

In another embodiment, the pH of the mixture is optionally adjusted toabout 7 with the addition of aqueous sodium hydroxide. In a furtherembodiment, the aqueous sodium hydroxide is a solution of about 1% toabout 40%, optionally about 5% to about 30%, by weight of sodiumhydroxide in water.

In another embodiment, the mixture is optionally milled using a wetmilling process. In an embodiment, the wet milling of the mixtureresults in thorough mixing of the defatted or protein-enriched meal withthe mixing solvent.

In another embodiment of the present disclosure, the mixture iscentrifuged using a decanting centrifuge. In an embodiment, the mixtureis centrifuged with a decanting centrifuge at a speed of about 1000 rpmto about 2000 rpm. In another embodiment, the speed is about 1500 rpm.

In another embodiment, the protein slurry is centrifuged using a discstack centrifuge to separate insoluble proteins from soluble proteins,forming a protein precipitate and a soluble protein fraction. In anembodiment, the soluble protein fraction is filtered as described above.In an embodiment, the disc centrifuge operates continuously at a speedof about 6500 rpm to about 8500 rpm at a temperature of about 1° C. toabout 60° C., optionally about 20° C. to about 40° C., or optionally atabout 20° C. to about 25° C.

In an embodiment of the disclosure, the precipitated protein is mixedwith water and its pH optionally adjusted for the addition of cellulasecomplex, in a similar manner as described above. This additionalenzymatic step hydrolyzes residual fiber and allows the removal of fiberfrom the protein precipitate.

In another embodiment, after treatment with the cellulase complex, theprotein precipitate is washed at least once with an extraction solventto remove water-soluble sugar compounds as a result of the fiberhydrolyzation by the cellulase complex. In an embodiment, the extractionsolvent is water. In an embodiment, the protein precipitate mixture iswashed at least twice with the extraction solvent. In an embodiment, theratio of extraction solvent to the precipitated protein is about 10:1 toabout 1:1, optionally about 4:1 to about 2:1. The mixture is thenfurther centrifuged to obtain a protein precipitate that has beenfurther purified.

In an embodiment, the further purified protein precipitate is thensubjected to high pressure jet cooking to obtain a high functionalprotein isolate having a protein content of greater than about 90% on adry weight basis. In an embodiment, the jet cooking of the proteinisolate occurs at a temperature of about 90° C. to about 120° C. forabout 1 second to about 2 minutes, optionally about 3 seconds to about30 seconds. As will be understood by a person skilled in the art, jetcooking involves the injection of steam into the purified protein, andresults in the pasteurization of the protein and improves the functionalproperties of the protein isolate.

In another embodiment, the further purified protein precipitate ishydrolyzed using proteases to form a hydrolyzed protein extractcontaining hydrolyzed proteins, peptides and amino acids having aprotein content of greater than about 90% on a dry weight basis. In anembodiment, the proteases are, for example, Alcalase® and Flavourzyme®.Alcalase® and Flavourzyme® were obtained from Novozymes North America,Inc., Franklinton, N.C. USA. This step hydrolyzes the protein in theprotein precipitate into smaller peptides and amino acids, which aresoluble in nutritional drinks and are easily adsorbed. In an embodiment,the purified protein precipitate is mixed with water to form a proteinslurry, which is optionally followed by pH adjustment to a pH of about6.0 to about 10.0, optionally about 7.5 to about 8.5. In an embodiment,the Alcalase® is added in a ratio of about 0.5% based on the dry weightof the protein slurry. In a further embodiment, the temperature isadjusted to about 20° C. to about 65° C., optionally about 50° C. toabout 60° C., or about 60° C., for about 1 to about 4 hours. Thehydrolyzed protein slurry is then cooled to about 30° C. to about 50°C., or about 40° C. to about 50° C., or about 50° C. The pH of themixture is then adjusted to a pH of about 5.0 to about 7.0, or about 6.0to about 7.0, or about 6.5, and a protease to form a hydrolyzed proteinextract, such as Flavourzyme®, is then added to the mixture. In anembodiment, the protease to form a hydrolyzed protein extract, such asFlavourzyme®, is added in a ratio of about 0.5% based on the dry weightof the protein slurry. In a further embodiment, the mixture is thenheated to a temperature of about 20° C. to about 60° C., optionallyabout 40° C. to about 60° C., or about 45° C. to about 55° C., for about1 to about 4 hours. The hydrolyzed protein mixture is then centrifugedto separate the hydrolyzed protein extract from the insoluble solids.The soluble hydrolyzed protein extract is then spray dried as describedabove, while the extract from the centrifugation is added to the solubleprotein fraction as described above.

In another embodiment of the disclosure, there is a provided a processfor the production of a protein concentrate from a partially defatted,fully defatted or protein-enriched meal, comprising:

-   -   i) mixing the partially defatted, fully defatted or        protein-enriched meal with a mixing solvent to form a mixture;    -   ii) optionally adjusting the pH of the mixture to a pH of about        2.0 to about 10.0;    -   iii) separating fiber from the mixture to form a protein slurry,        wherein the protein slurry comprises a soluble protein fraction        and an insoluble protein fraction;    -   iv) optionally repeating steps i)-iii) by mixing the protein        slurry with additional partially defatted, fully defatted or        protein-enriched meal;    -   v) mixing the protein slurry with an extraction solvent to form        an extract and a washed insoluble protein fraction;    -   vi) separating the extract from the washed insoluble protein        fraction;    -   vii) optionally repeating steps v) and vi) at least once; and    -   viii) desolventizing the washed insoluble protein fraction to        form a protein concentrate.

In another embodiment of the disclosure, the ratio of partiallydefatted, fully defatted or protein-enriched meal to mixing solvent isabout 1:3 to about 1:30 (w/w). In another embodiment, the ratio ofpartially defatted, fully defatted or protein-enriched meal to solventis about 1:5 to about 1:20 (w/w). In a further embodiment, the ratio isabout 1:6 to about 1:12 (w/w). In an embodiment, the ratio is about 1:8to about 1:10 (w/w).

In a further embodiment of the disclosure, the mixing solvent compriseswater or an aqueous solution comprising a polysaccharide, a salt or analcohol. In an embodiment, the mixing solvent is water. In anotherembodiment, the polysaccharide is guar gum.

In an embodiment, the pH of the protein slurry is adjusted to a pH ofabout 6.5 to about 10.0. In a further embodiment, the pH of the proteinslurry is adjusted to a pH of about 7.0 to about 9.0.

In an embodiment, the mixture is centrifuged to separate the fiber frommixture and form the protein slurry. In an embodiment, the mixture iscentrifuged at a speed of about 1,000 rpm to about 2,000 rpm. In afurther embodiment, the mixture is centrifuged at a speed of about 1,400to about 1,600 rpm. In an embodiment, the mixture is centrifuged using adecanter centrifuge.

The centrifugation of the mixture results in three layers: i) aninsoluble fiber layer and a protein slurry on top of the fiber, whichwas comprised of ii) an insoluble protein fraction and iii) a solubleprotein fraction. Separation of the top and middle layers (the solubleprotein extract and the insoluble fine protein fraction) from the bottomlayer (coarse fiber solids), resulted in the protein slurry with fiberremoved. In an embodiment, the bird decanter was operated at a low pooldepth with a bowl speed of between about 1,000 rpm and about 2,000 rpm,optionally 1,400 to about 1,600 rpm, suitably about 1,500 rpm. It wasdetermined that when the speed of the centrifugation is too high, forexample at 5,000 rpm, the insoluble protein fraction settles with thefiber. If the speed of the centrifugation is too low, fiber will remainin the protein slurry. Accordingly, in an embodiment, when the speed ofthe centrifugation is between about 1,000 rpm and about 2,000 rpm,optionally 1,400 to about 1,600 rpm, suitably about 1,500 rpm, the fiberin the mixture is separated from both the soluble and insoluble protein.

In another embodiment of the disclosure, mixing the protein slurry withadditional partially defatted, fully defatted or protein-enriched mealis repeated at least once. In a further embodiment, mixing the proteinslurry with additional partially defatted, fully defatted orprotein-enriched meal is repeated at least two to seven times. In anembodiment, recycling the protein slurry with additional partiallydefatted, fully defatted or protein-enriched meal increases the solidcontent of the meal being processed, and accordingly, reduces theoverall processing volume.

In an embodiment of the disclosure, the extraction solvent compriseswater, methanol, ethanol, isopropanol, or mixtures thereof. In anembodiment, the extraction solvent comprises ethanol. In anotherembodiment, the extraction solvent comprises at least about 50% ethanol.In an embodiment, the extraction solvent comprises at least about 70%ethanol. In a further embodiment, the extraction solvent comprises atleast about 90% ethanol.

In a further embodiment, the extract is separated from the washedinsoluble protein fraction using centrifugation, vacuum filtration,pressure filtration, decantation or gravity draining. In an embodiment,the extract is separated from the washed insoluble protein fractionusing centrifugation.

In another embodiment of the disclosure, wherein steps iv) and v) arerepeated at least twice.

In a further embodiment, the process further comprises the step ofdrying the washed insoluble protein fraction to form the proteinconcentrate. In an embodiment, the protein concentrate is dried in avacuum dryer, fluidized bed dryer, hot air dryer ring dryer or spraydryer.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched meal comprises a canola, rapeseed, mustardseed, broccoli seed, flax seed, cotton seed, hemp seed, safflower seed,sesame seed or soybean meal. In another embodiment, the partiallydefatted, fully defatted or protein-enriched meal comprises a canolameal.

In an embodiment, the protein concentrate comprises a protein content ofabout 60% to about 90% on a dry weight basis.

In another embodiment of the disclosure, there is also provided aprocess for the production of a protein isolate from a partiallydefatted, fully defatted or protein enriched meal, comprising:

-   -   i) mixing the partially defatted, fully defatted or        protein-enriched meal with alkaline water to form a mixture;    -   ii) optionally adjusting the pH of the mixture to a pH of about        6.0 to about 10.0;    -   iii) separating fiber from the mixture to form a first protein        slurry, wherein the first protein slurry comprises a soluble        protein fraction and an insoluble protein fraction;    -   iv) separating the first protein slurry to form a protein solids        fraction and a soluble protein fraction;    -   v) mixing the protein solids fraction with water to form a        second protein slurry;    -   vi) separating the second protein slurry to form a second        protein solids fraction and a second soluble protein fraction;    -   vii) optionally repeating steps v) and vi) at least once;    -   viii) separating the soluble protein fractions to form a        clarified soluble protein fraction and a residual insoluble        protein fraction;    -   ix) optionally adjusting the pH of the clarified soluble protein        fraction to a pH of about 7;    -   x) separating the clarified soluble protein fraction, optionally        by filtering the clarified soluble protein fraction by membrane        filtration; and        xi) optionally drying the clarified soluble protein fraction.

In another embodiment of the disclosure, the ratio of partiallydefatted, fully defatted or protein-enriched meal to alkaline water isabout 1:3 to about 1:30 (w/w). In another embodiment, the ratio ofpartially defatted, fully defatted or protein-enriched meal to alkalinewater is about 1:5 to about 1:20 (w/w). In a further embodiment, theratio is about 1:6 to about 1:12 (w/w). In an embodiment, the ratio isabout 1:8 to about 1:10 (w/w).

In an embodiment of the disclosure, the pH of the alkaline water isabout 7 to about 12. In another embodiment, the pH of the first proteinslurry is adjusted to about 8.0 to about 9.5. In a further embodiment,the pH of the first protein slurry is adjusted to about 8.5 to about9.0.

In an embodiment, the mixture is centrifuged to separate the fiber fromthe protein slurry and form the protein extract. In an embodiment, themixture is centrifuged at a speed of about 1,000 rpm to about 2,000 rpm.In a further embodiment, the mixture is centrifuged at a speed of about1,400 to about 1,600 rpm. In an embodiment, the mixture is centrifugedusing a decanter centrifuge.

In another embodiment, the first protein slurry is centrifuged toseparate the protein solids fraction from the soluble protein fraction.In a further embodiment, the first protein slurry is centrifuged at aspeed of about 4,000 rpm to about 8,500 rpm. In a further embodiment,the first protein slurry is centrifuged at a speed of about 5,000 toabout 8,500 rpm.

In another embodiment of the disclosure, the ratio of the protein solidsfraction to water is about 1.0:0.5 to about 1.0:3.0 (w/w). In a furtherembodiment, the ratio of the protein solids fraction to water is about1.0:1.0 to about 1.0:2.0 (w/w).

In an embodiment, the soluble protein fractions are centrifuged to formthe clarified soluble protein fraction and the residual insolubleprotein fraction. In an embodiment, the soluble protein fractions arecentrifuged using a disc stack centrifuge at a speed of about 7,000 rpmto about 10,000 rpm. In a further embodiment, the soluble proteinfractions are centrifuged using a disc stack centrifuge at a speed ofabout 8,400 rpm to about 8,600 rpm.

In another embodiment of the disclosure, the pH of the clarified solubleprotein fraction is adjusted with alkali. In a further embodiment, thepH of the clarified soluble protein fraction is adjusted with sodiumhydroxide.

In an embodiment, the clarified soluble protein fraction is filteredusing an ultrafiltration apparatus. In a further embodiment, theultrafiltration apparatus comprises a membrane to filter proteins largerthan about 10,000 daltons. In another embodiment, the separation of theclarified soluble protein fraction is accomplished by adjusting the pHof the solution to the isoelectric point of the proteins (about pH of4.5), and consequently, the proteins are precipitated out of solution.In another embodiment, the proteins are cooked to precipitate theproteins from solution.

In another embodiment of the disclosure, the process further comprisesthe step of filtering the clarified soluble protein fraction using adiafiltration apparatus.

In another embodiment, the clarified soluble protein fraction is driedin a vacuum dryer, fluidized bed dryer, freeze dryer, ring dryer orspray dryer to form the protein isolate.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched meal comprises a canola, rapeseed, mustardseed, broccoli seed, flax seed, cotton seed, hemp seed, safflower seed,sesame seed or soybean meal. In another embodiment, the partiallydefatted, fully defatted or protein-enriched meal comprises a canolameal.

In another embodiment of the disclosure, the protein concentratecomprises a protein content of greater than about 90% on a dry weightbasis.

In another embodiment of the disclosure, there is also provided aprocess for the production of a hydrolyzed protein concentrate from apartially defatted, fully defatted or protein-enriched meal, comprising:

-   -   i) mixing the partially defatted, fully defatted or        protein-enriched meal with water to form a mixture;    -   ii) optionally adjusting the pH of the mixture to a pH of about        6.0 to about 10.0;    -   iii) separating the mixture to remove fiber from the mixture and        form a first protein slurry, wherein the first protein slurry        comprises a soluble protein fraction and an insoluble protein        fraction;    -   iv) optionally adjusting the pH of the first protein slurry to a        pH of about 7.0;    -   v) separating the first protein slurry to form a first protein        solids fraction and a first soluble protein fraction;    -   vi) mixing the first protein solids fraction with water to form        a second protein slurry;    -   vii) separating the second protein slurry to form a second        protein solids fraction and a second soluble protein fraction;    -   viii) mixing the second protein solids fraction with water to        form a third protein slurry;    -   ix) adjusting the pH of the third protein slurry to a pH of        about 7.0 to about 9.0;    -   x) mixing the third protein slurry with at least one protease to        form a hydrolyzed protein extract;    -   xi) separating the hydrolyzed protein extract from the third        protein slurry to form the hydrolyzed protein concentrate.

In another embodiment of the disclosure, the ratio of partiallydefatted, fully defatted or protein-enriched meal to water is about 1:3to about 1:30 (w/w). In another embodiment, the ratio of partiallydefatted, fully defatted or protein-enriched meal to water is about 1:5to about 1:20 (w/w). In a further embodiment, the ratio is about 1:6 toabout 1:12 (w/w). In an embodiment, the ratio is about 1:8 to about 1:10(w/w).

In another embodiment, the pH of the mixture is adjusted to about 8.0 toabout 9.0. In a further embodiment, the pH of the mixture is adjusted toabout 8.5 to about 9.0.

In an embodiment, the mixture is centrifuged to separate the fiber fromthe protein slurry and form the protein extract. In an embodiment, themixture is centrifuged at a speed of about 1,000 rpm to about 2,000 rpm.In a further embodiment, the mixture is centrifuged centrifuge at aspeed of about 1,400 to about 1,600 rpm. In an embodiment, the mixtureis centrifuged using a decanter centrifuge.

In another embodiment, the first protein slurry is centrifuged toseparate the protein solids fraction from the soluble protein fraction.In a further embodiment, the first protein slurry is centrifuged at aspeed of about 4,000 rpm to about 8,000 rpm. In a further embodiment,the first protein slurry is centrifuged at a speed of about 5,000 toabout 8,500 rpm.

In another embodiment, the ratio of the first and second protein solidsfraction to water is about 1.0:0.5 to about 1.0:3.0 (w/w). In a furtherembodiment, the ratio of the first and second protein solids fraction towater is about 1.0:1.0 to about 1.0:2.0 (w/w).

In another embodiment of the disclosure, the pH of the third proteinslurry is adjusted to about 8.0 to about 8.5.

In an embodiment of the disclosure, the ratio of the third proteinslurry to the protease is about 100:1 to about 5000:1 (w/w).

In an embodiment of the disclosure, the third protein slurry is mixedwith a protease at a temperature of about 50° C. to about 70° C. Inanother embodiment, the third protein slurry is mixed with a protease ata temperature of about 55 to about 65° C.

In another embodiment, the at least one protease comprises a proteasefrom Bacillus Licheniformis.

In a further embodiment, the process further comprises the step ofmixing the third protein slurry with a second protease.

In an embodiment, the ratio of the third protein slurry to the secondprotease is about 100:1 to about 5000:1 (w/w).

In another embodiment, the third protein slurry is mixed with the secondprotease at a temperature of about 40° C. to about 60° C. In anembodiment, the third protein slurry is mixed with the second proteaseat a temperature of about 45° C. to about 55° C.

In a further embodiment, the second protease comprises a fungalprotease/peptidase complex from Aspergillus oryzae.

In an embodiment, the hydrolyzed protein extract is separated using acentrifuge. In a further embodiment, the hydrolyzed protein extract isseparated using a decanter centrifuge at a speed of about 3,800 to about5,200 rpm.

In another embodiment, the clarified soluble protein fraction is driedin a vacuum dryer, fluidized bed dryer, ring dryer or spray dryer toform the protein isolate.

In an embodiment of the disclosure, the partially defatted, fullydefatted or protein-enriched meal comprises a canola, rapeseed, mustardseed, broccoli seed, flax seed, cotton seed, hemp seed, safflower seed,sesame seed or soybean meal. In another embodiment, the partiallydefatted, fully defatted or protein-enriched meal comprises a canolameal.

In a further embodiment, the hydrolyzed protein concentrate comprises aprotein content of greater than about 70% on a dry weight basis.

In an embodiment, the use of an extraction solvent, such as ethanol,leads to a protein concentrate or protein isolate having superiororganoleptic properties, as well as superior protein solubilityproperties, which therefore possesses better functional properties. Inan embodiment, the use of an extraction solvent, such as ethanol,results in the protein concentrates containing fewer impurities.Consequently, the protein concentrates are generally of higher qualityand have better functional properties.

The present disclosure relates to processes for the production ofprotein concentrates and protein isolates, in which the oilseed meal issubjected to low g-forces to separate the fiber from the insoluble andsoluble protein fractions. Removing the fiber from a protein mixtureusing low g-forces, separates the insoluble fiber from the proteinfraction, and in particular the insoluble protein fraction, whichconsequently increases the amount of recoverable protein from an oilseedmeal.

Accordingly, the present disclosure includes a process for theproduction of a protein concentrate from an oilseed meal comprising:

i) mixing the oilseed meal with a first blending solvent to form amixture;

ii) optionally treating the mixture with phytase at a temperature and apH suitable for phytase activity;

iii) optionally adjusting the pH of the mixture to a pH between 6.0 and10.0;

iv) subjecting the mixture to a g-force sufficient to separate themixture to form

-   -   a) a fiber fraction, and    -   b) protein fractions comprising an insoluble protein fraction        and a soluble protein fraction;

v) optionally mixing the fiber fraction with a second blending solventand repeating step iv);

vi) optionally adjusting the pH of the protein fraction to a pH between4.0 and 6.0;

vii) heating the protein fraction to a temperature between 80° C. and100° C. to precipitate the proteins; and

viii) separating the precipitated proteins from the protein fraction toform the protein concentrate.

In another embodiment, the first and second blending solvents comprisewater, a saline solution or a polysaccharide solution. In a furtherembodiment, the first and second blending solvents comprise water.

In an embodiment of the disclosure, the ratio of the oilseed meal to thefirst blending solvent is 1:3 to 1:30 (w/w) of meal to water, optionallyabout 1:8 to about 1:10 (w/w).

In an embodiment, the temperature suitable for phytase activity isbetween 20° C. and 60° C., optionally between 40° C. and 55° C.,suitably between 50° C. and 55° C. In another embodiment, the pHsuitable for phytase activity is between 2.0 and 7.0, optionally between4.0 and 6.0, suitably between 4.5 and 5.5, optionally 5.0 to 5.5. Inanother embodiment, the concentration of the phytase enzyme is between0.01% to 1.0% (w/w) based on the weight of the oilseed meal, optionally0.01% and 0.5% optionally 0.01% and 0.1%. In another embodiment, themixture is incubated with the phytase enzyme under good agitation. Theaddition of phytase enzyme to the protein mixture results in thehydrolysis of phytates and/or phytic acid present in the oilseed meal toorganic phosphates and inositol. It is known to those skilled in the artthat phytates and phytic acid may constitute undesirableanti-nutritional compounds in a protein meal, and accordingly, aredesirably removed from the oilseed meal and the final protein products.Accordingly, the addition of phytase enzyme results in the hydrolysis ofthe phytates and/or phytic acid which are subsequently removed from themixture. In addition, it has also been determined that phytates and/orphytic acid complex with proteins to form an insoluble gel complex.Accordingly, in an embodiment, when filtration, such as diafiltration orultrafiltration, is utilized to purify and separate protein concentratesand/or protein isolates, the insoluble protein/phytate (or phytic acid)gel complexes block the filtration apparatus, reducing the flow throughthe filtration apparatus, and accordingly, reducing the amount ofrecoverable protein and filtration efficiency. It will be understoodthat the addition of phytase to the mixture and the conditions recitedfor reduction or removal of phytates and/or phytic acid apply to all ofthe processes and embodiments of the present disclosure.

In another embodiment of the disclosure, after treating the mixture withthe phytase enzyme, the pH of the mixture is optionally adjusted to a pHof about 6.0 to about 10.0, optionally 6.5 to about 9.5, suitably 7.0 to8.0, using a base, such as sodium hydroxide, potassium hydroxide, etc.In an embodiment, adjusting the pH of the mixture results in the proteinbecoming more soluble in the blending solvent, such as water, whichconsequently increases the yield of the protein concentrate.

In another embodiment of the disclosure, the mixture is subjected to ag-force sufficient to separate the mixture to form a fiber fraction andprotein fractions comprising an insoluble protein fraction and a solubleprotein fraction. The separation of the mixture using a sufficientg-force is described herein with reference to a centrifuge, such as adecanter centrifuge or a disc stack centrifuge, but a person skilled inthe art would understand that other methods of separation that create aseparation force, including a hydrocyclone, are also included.Accordingly, in an embodiment, when the mixture is subjected to asufficient g-force using a centrifuge, the mixture separates intothree-phases as a result of the sedimentation principle: (i) aninsoluble fiber fraction, and (ii) protein fractions comprising (ii.a)an insoluble protein fraction, and (ii.b) a soluble protein fraction.The centripetal acceleration acting on the mixture results in theinsoluble fiber fraction, which has a relatively higher density and/orgreater particle size compared to the other fractions, moving furtheralong the radial direction in which the centripetal force is acting(perpendicular to the axis of rotation). When a centrifuge is utilized,the insoluble fiber fraction (or phase) moves towards the bottom of thecentrifuge tube, as a result of its relatively higher density and/orgreater particle size, resulting in one of the phases of separation. Asa result of the proteins in the insoluble protein fraction having alower relative density and/or smaller particle size as compared to theinsoluble fiber fraction, the insoluble protein fraction forms anotherphase of separation (the middle phase). Finally, the proteins in thesoluble protein fraction, being soluble in the blending solvent and/orhaving a lower relative density compared to the fiber fraction andinsoluble protein fraction, remain near the top of the centrifuge tube.If oil seed meal is partially defatted meal, a fourth phase may alsoform on top of the soluble protein phase comprising residual oil. Itwill be understood that subjecting the mixture to a sufficient g-forcewill not result in a total separation of the three fractions, andaccordingly, a minor amount of fiber will be present in the proteinfraction, while protein will be present in the insoluble fiber fraction.There will be a certain amount of protein trapped within the structureof the insoluble fiber fraction that is not separable using mechanicalmeans (i.e. using a centrifuge). In an embodiment, the amount of proteintrapped within the fiber fraction will be 30%, optionally 20%, 10%, 5%,1%. In another embodiment, proteases (such as Protames, Alcalase 2.4 LFG and/or Flavourzyme 1000 L) are used to hydrolyze the protein trappedwithin the fiber fraction, which releases the protein from the fiber,and can be recovered therefrom, and such a process is also included inthe present disclosure. In this embodiment, the hydrolyzed protein isseparated from the fiber using any of the means disclosed herein (e.g.centrifugation, hydrocyclone). It will be understood that the disclosureconcerning the g-force sufficient to separate the mixture as describedabove applies to all of the processes and embodiments of the presentdisclosure.

In an embodiment, the mixture is subjected to a g-force of between 100 gand 500 g, suitably between 150 g and 400 g, optionally between 180 gand 350 g. Calculation of g-force (or relative centrifugal force)optionally involves the RPMs (revolutions per minute) of the device, aswell as the rotational radius (in centimeters):

g-force=(RPM)²*(rotational radius)*(0.00001118)

A person skilled in the art will readily be able to calculate theg-force from the RPMs of a given separation device, such as a centrifugeor a hydrocyclone.

In another embodiment, separating the mixture comprises using acentrifuge or a hydrocyclone. In another embodiment, the centrifugecomprises a decanter centrifuge or a disc stack centrifuge.

In another embodiment, as there will be a residual amount of protein inthe separated fiber fraction, the separated fiber fraction is washedwith a second blending solvent, optionally at least once, optionallytwice or more than twice, and the mixture is then again subjected to ag-force to separate the mixture to form a fiber fraction and a proteinfraction comprising an insoluble protein fraction and a soluble proteinfraction.

In another embodiment, the separation of the insoluble fiber fractionfrom the protein fractions, results in fiber solids which are dried andconsequently constitute a high fiber canola meal containing a lowconcentration of anti-nutritional factors, such as phytates and/orphytic acid.

In another embodiment, the pH of the protein fraction comprising theinsoluble protein fraction and soluble protein fraction is adjustedusing an acid, such as phosphoric acid, nitric acid, citric acid,sulfuric acid, and the pH is adjusted to between 4.0 and 6.0, optionally4.0 and 5.0, suitably 4.0 and 4.5. In an embodiment, adjusting the pH ofthe protein fraction using an acid results in undesirable ash becomingsoluble in the protein fraction, and therefore, separable from the finalprotein concentrate.

In another embodiment, the protein fraction comprising the insolubleprotein fraction and the soluble protein fraction is heated to atemperature between 80° C. and 100° C., optionally 90° C. and 100° C.,suitably 95° C. and 100° C., for a time period of between 5 minutes and60 minutes, optionally 5 minutes and 45 minutes, suitably between 10minutes and 30 minutes. Increasing the temperature of the proteinfractions denatures some of the undenatured proteins in the solubleprotein fraction, rendering them insoluble, and therefore increasing theyield of the insoluble protein concentrate.

In a further embodiment, separating the precipitated proteins comprisesusing a centrifuge or a hydrocyclone. In another embodiment, separatingthe precipitated proteins comprises using a centrifuge, such as decantercentrifuge or a disc stack centrifuge. In another embodiment,centrifuging the precipitated proteins comprises a g-force between 2,500g and 9,500 g. When the centrifuge is operated at such a g-force, theprecipitated proteins move along the radial axis to the bottom of thecentrifuge tube and are easily separated from the supernatant.

In another embodiment of the disclosure, the process further comprisingthe step of drying the protein concentrate to a moisture content ofbetween 4% and 8%, optionally 6% (w/w). In another embodiment, thedrying is performed using a fluidized bed dryer, conveyor dryer, rotarydryer, drum dryer, spray drier or a ring drier.

In another embodiment, there is also included a protein concentratehaving a protein content of at least 60% and less than 90% proteincomprising:

i) a first protein fraction comprising between 30% and 70% 2S protein,optionally between 40% and 60%, optionally 45% and 55%;

ii) a second protein fraction comprising between 20% and 50% 12Sprotein, optionally between 25% and 45%, optionally between 30% and 40%,optionally between 35% and 40%.

In another embodiment, the protein concentrate comprises a hydrolyzedprotein concentrate. In another embodiment, the hydrolyzed proteinconcentrate comprises peptides and/or free amino acids.

The present disclosure also includes a process for the production of aprotein concentrate from an oilseed meal comprising:

i) mixing the oilseed meal with a first blending solvent to form amixture;

ii) optionally treating the mixture with phytase at a temperature and apH suitable for phytase activity; iii) optionally adjusting the pH ofthe mixture to a pH between 6.0 and 10.0;

iv) subjecting the mixture to a g-force sufficient to separate themixture to form

-   -   a) a fiber fraction, and    -   b) protein fractions comprising an insoluble protein fraction        and a soluble protein fraction;

v) optionally mixing the fiber fraction with a second blending solventand repeating step iv);

vi) optionally adjusting the pH of the protein fraction to a pH between4.0 and 6.0;

vii) mixing the protein fraction with a mixing solvent to form a proteinslurry and precipitate the proteins;

viii) separating the precipitated proteins from the protein slurry toform the protein concentrate; and

ix) optionally repeating steps vii) and viii) with the precipitatedproteins.

In another embodiment, the first and second blending solvents comprisewater, a saline solution or a polysaccharide solution. In a furtherembodiment, the first and second blending solvents comprise water.

In an embodiment of the disclosure, the ratio of the oilseed meal to thefirst blending solvent is 1:3 to 1:30 (w/w) of meal to water, optionallyabout 1:8 to about 1:10 (w/w).

In an embodiment, the temperature suitable for phytase activity isbetween 20° C. and 60° C., optionally between 40° C. and 55° C.,suitably between 50° C. and 55° C. In another embodiment, the pHsuitable for phytase activity is between 2.0 and 7.0, optionally between4.0 and 6.0, suitably between 4.5 and 5.5, optionally 5.0 to 5.5. Inanother embodiment, the concentration of the phytase enzyme is between0.01% to 1.0% (w/w) based on the weight of the oilseed meal, optionally0.01% and 0.5% optionally 0.01% and 0.1%. In another embodiment, themixture is incubated with the phytase enzyme under good agitation.

In another embodiment of the disclosure, after treating the mixture withthe phytase enzyme, the pH of the mixture is optionally adjusted to a pHof about 6.0 to about 10.0, optionally 6.5 to about 9.5, suitably 7.0 to8.0, using a base, such as sodium hydroxide, potassium hydroxide, etc.In an embodiment, adjusting the pH of the mixture results in the proteinbecoming more soluble in the blending solvent, such as water, whichconsequently increases the yield of the protein concentrate.

In another embodiment of the disclosure, the mixture is subjected to ag-force of between 100 g and 500 g, suitably between 150 g and 400 g,optionally between 180 g and 350 g.

In another embodiment, separating the mixture comprises using acentrifuge or a hydrocyclone. In another embodiment, the centrifugecomprises a decanter centrifuge or disc stack centrifuge.

In another embodiment, as there will be a residual amount of protein inthe separated fiber fraction, the separated fiber fraction is washedwith a second blending solvent, optionally at least once, optionallytwice or more than twice, and the mixture is then again subjected to ag-force to separate the mixture to form a fiber fraction and a proteinfraction comprising an insoluble protein fraction and a soluble proteinfraction.

In another embodiment, the separation of the insoluble fiber fractionfrom the protein fraction, results in fiber solids which are dried andconsequently constitute a high fiber canola meal containing a lowconcentration of anti-nutritional factors, such as phytates and/orphytic acid.

In another embodiment, the pH of the protein fraction comprising theinsoluble protein fraction and soluble protein fraction is adjustedusing an acid, such as phosphoric acid, nitric acid, citric acid,sulfuric acid, hydrochloric acid, and the pH is adjusted to between 4.0and 6.0, optionally 4.0 and 5.0, suitably 4.0 and 4.5. In an embodiment,adjusting the pH of the protein fraction using an acid results inundesirable ash becoming soluble in the protein fraction, and therefore,separable from the final protein concentrate.

In another embodiment of the disclosure, the protein fraction is mixedwith a mixing solvent comprising an ethanol:water mixture, wherein theethanol is present in an amount between 80% and 100%, optionally 85% and100% (v/v), optionally 90% and 100% (v/v), optionally 95% and 100%(v/v). It will be understood that 100% ethanol may contain a smallpercentage of impurities such as water, etc., which cannot be removedfrom the ethanol. In an embodiment, mixing solvent is added to theprotein fraction at a ratio of between 2:1 and 1:2 (v/v of mixingsolvent:protein fraction), optionally 1:1. In an embodiment, when themixing solvent comprises an alcohol, such as ethanol (80%, 90%, 95%ethanol in water or 100% ethanol), proteins in the protein slurryprecipitate from solution, as a result the proteins being less solublein the mixing solvent (such as ethanol) than in the blending solvent(such as water), and therefore increases the yield of the proteinconcentrate.

In another embodiment, separating the precipitated proteins comprisesusing a centrifuge or a hydrocyclone. In another embodiment, separatingthe precipitated proteins comprises using a centrifuge, such as decantercentrifuge or disc stack centrifuge. In another embodiment, centrifugingthe precipitated proteins comprises a g-force between 2,500 g and 9,500g. When the centrifuge is operated at such a g-force, the precipitatedproteins move along the radial axis to the bottom of the centrifuge tubeand are easily separated from the supernatant.

In another embodiment of the disclosure, steps viii) and viii) arerepeated at least twice, such that the precipitated proteins are washedwith mixing solvent to remove impurities.

In another embodiment, the process further comprises the step of dryingthe protein concentrate to a moisture content of between 4% and 8%(w/w), optionally 6% (w/w). In another embodiment, the drying isperformed using a fluidized bed dryer, spray dryer or a ring drier.

In another embodiment, there is also included a protein concentratehaving a protein content of at least 60% and less than 90% proteincomprising:

i) a first protein fraction comprising between 30% and 70% 2S protein,optionally between 40% and 60%, optionally 45% and 55%;

ii) a second protein fraction comprising between 20% and 50% 12Sprotein, optionally between 25% and 45%, optionally between 30% and 40%,optionally between 35% and 40%.

In another embodiment, the protein concentrate comprises a hydrolyzedprotein concentrate. In a further embodiment, the hydrolyzed proteinconcentrate comprises peptides and/or free amino acids.

The present disclosure also includes a process for the production of aprotein isolate from an oilseed meal comprising:

i) mixing the oilseed meal with a first blending solvent to form amixture;

ii) optionally treating the mixture with phytase at a temperature and apH suitable for phytase activity;

iii) optionally adjusting the pH of the mixture to a pH between 6.0 and10.0;

iv) subjecting the mixture to a g-force sufficient to separate themixture to form

-   -   a) a fiber fraction, and    -   b) protein fractions comprising an insoluble protein fraction        and a soluble protein fraction;

v) optionally mixing the fiber fraction with a second blending solventand repeating step iv);

vi) separating the insoluble protein fraction from the soluble proteinfraction to recover therefrom an insoluble protein concentrate and asoluble protein extract; and

vii) subjecting the soluble protein extract to filtration to recovertherefrom the protein isolate.

In another embodiment, the first and second blending solvents comprisewater, a saline solution or a polysaccharide solution. In a furtherembodiment, the first and second blending solvents comprise water.

In an embodiment of the disclosure, the ratio of the oilseed meal to thefirst blending solvent is 1:3 to 1:30 (w/w) of meal to water, optionally1:8 to 1:10 (w/w).

In an embodiment, the temperature suitable for phytase activity isbetween 20° C. and 60° C., optionally between 40° C. and 55° C.,suitably between 50° C. and 55° C. In another embodiment, the pHsuitable for phytase activity is between 2.0 and 7.0, optionally between4.0 and 6.0, suitably between 4.5 and 5.5, optionally 5.0 and 5.5. Inanother embodiment, the concentration of the phytase enzyme is between0.01% and 1.0% (w/w) based on the weight of the oilseed meal, optionally0.01% and 0.5% optionally 0.01% and 0.1%. In another embodiment, themixture is incubated with the phytase enzyme under good agitation.

In another embodiment of the disclosure, after treating the mixture withthe phytase enzyme, the pH of the mixture is optionally adjusted to a pHof between 6.0 and about 10.0, optionally 7.0 and 9.0, suitably 7.0 and8.0, using a base, such as sodium hydroxide, potassium hydroxide, etc.In an embodiment, adjusting the pH of the mixture results in the proteinbecoming more soluble in the blending solvent, such as water, whichconsequently increases the yield of the protein isolate.

In another embodiment of the disclosure, the mixture is subjected to ag-force of between 100 g and 500 g, suitably between 150 g and 400 g,optionally between 180 g and 350 g.

In another embodiment, separating the mixture comprises using acentrifuge or a hydrocyclone. In an embodiment, the centrifuge comprisesa decanter centrifuge or disc stack centrifuge.

In another embodiment, as there will be a residual amount of protein inthe separated fiber fraction, the separated fiber fraction is washedwith a second blending solvent, optionally at least once, optionallytwice or more than twice, and the mixture is then again subjected to ag-force to separate the mixture to form a fiber fraction and a proteinfraction comprising an insoluble protein fraction and a soluble proteinfraction.

In another embodiment, the separation of the insoluble fiber fractionfrom the protein fraction, results in fiber solids which are dried andconsequently constitute a high fiber canola meal containing a lowconcentration of anti-nutritional factors, such as phytates and/orphytic acid.

In another embodiment, separating the insoluble protein fraction fromthe soluble fiber fraction comprises using a centrifuge or ahydrocyclone. In a further embodiment separating the insoluble proteinfraction from the soluble protein fraction comprises using a centrifuge,such as a decanter centrifuge or disc stack centrifuge.

In another embodiment, centrifuging to separate the insoluble proteinfraction from the soluble protein fraction comprises a g-force between2,500 g and 9,500 g. In another embodiment, the separation of theinsoluble protein fraction from the soluble protein fraction results ina wet protein concentrate that can be subsequently dried. The extractfrom the separation of the insoluble protein fraction from the solubleprotein fraction comprises the soluble protein, which is subsequentlyfiltered through a filtration apparatus, such as ultrafiltration and/ordiafiltration, resulting in the protein isolate. As described above,phytates and/or phytic acid can complex and bind to the proteins, andconsequently block the filtration apparatus. The removal of the phytatesand/or phytic acid from the oilseed meal mixture (oilseed meal andblending solvent) using phytase as described above, such that thefiltration apparatus is not blocked with such complexes, resulting thefiltration apparatus performing efficiently to produce the proteinisolate.

In another embodiment, the process further comprises the step of dryingthe protein isolate to a moisture content of between 4% and 8% (w/w),optionally 6% (w/w). In another embodiment, the drying is performedusing a spray drier or a ring drier.

In another embodiment, there is also included a protein isolate having aprotein content of at least 90% protein comprising:

i) a first protein fraction comprising between 10% and 40% 2S protein,optionally between 15% and 30%;

ii) a second protein fraction comprising between 30% and 70% 12Sprotein, optionally 40% and 60%, optionally between 50% and 60%.

In a further embodiment, the protein isolate comprises a hydrolyzedprotein isolate. In another embodiment, the hydrolyzed proteinconcentrate comprises peptides and/or free amino acids.

Terms of degree such as “substantially”, “about” and “approximately” asused herein mean a reasonable amount of deviation of the modified termsuch that the end result is not significantly changed. These terms ofdegree should be construed as including a deviation of at least ±5% ofthe modified term if this deviation would not negate the meaning of theword it modifies.

The following non-limiting examples are illustrative of embodiments ofthe present disclosure:

EXAMPLES Reagents and Materials

Canola seeds (Brassica juncea and Brassica napus) were obtained fromViterra, North Battleford, Saskatchewan, Canada. Commercial methylpentane was purchased from Univar Canada Ltd., Saskatoon, Saskatchewan,Canada. Enzyme samples of Cellulase (Celluclast® 1.5 L), CellulaseComplex, Alcalase® 2.4 L FG, and Flavourzyme® were obtained fromNovozymes North America, Inc., Franklinton, N.C. USA. Pea proteinisolate was obtained from Roquette America, Inc., Keokuk, Iowa, USA. Soyprotein isolate was obtained from Protient, ABF Ingredients Company, St.Paul, Minn., USA

Analysis

Mixing of the materials was performed using a Ribbon Blender (TorcoModel R-12, Toronto Coppersmithing International Ltd., Scarborough,Ontario, Canada). Heat treatments of seed samples were conducted usingan Infra Red Cereal Processing System (Micronizing Company Limited,Framlingham, Sulfolk, England) or a two-tray Simon-Rosedown cooker(Laboratory cooker-press, Simon-Rosedowns Limited, Hull, England).Pressing of the oil seeds is performed using a Gusta Laboratory ScrewPress. Ultrafiltration was carried out using a Millipore®Ultrafiltration Unit (Model A60, Millipore® Corporation, Bedford, Mass.,USA). Protein content of the samples was determined by the Leco® ProteinAnalyzer (Model FP-428, Leco® Corporation, ST. Joseph, Mich. U.S.A.)based on AOCS Official Method Ba 4e-93. Moisture content of the sampleswas determined by drying samples in a 105±2° C. convection oven for 16hours or to a constant weight based on AOCS Official Method Ba 2a-38.Oil content of the samples was determined based on AOCS Official MethodBa 3-38 with the following changes: (a) 2 g of sample was used insteadof 5 g in the analysis; (b) extraction continued for 4 hours, and (c)extraction flask was heated to remove residual petroleum ethers. Ashcontent of the samples was determined based on AOCS Official Method Ba5a-49 with the following changes: (a) samples were pre-ashed on a hotplate prior to being placed into the muffle furnace; (b) samples wereincinerated for 18 hours in muffle furnace; and (c) nitric acid wasadded if sample remained black. Crude fiber content of the samples wasdetermined based on AOCS Official Method Ba 6-84 with the followingchanges: (a) samples with oil contents below 3% were not defatted and(b) digest was dried for 2 hours at 130° C. Protein dispersibility index(PDI) of the samples was determined based on A.O.C.S. Official Method Ba10-65. Free fatty acid (FFA) of the oil samples was determined based onAOCS Official Method Ca 5a-40. Phosphorus and sulphur of the sampleswere determined based on the modified methods of AOCS Ca20-99 and AOCSCa 17-01 (modified), respectively. Crude fiber content of the sampleswas determined based on AOCS Official Method Ba 6-84 with the followingchanges: (a) samples with oil contents below 3% were not defatted and(b) digest was dried for 2 hours at 130° C. Protein dispersibility index(PDI) of the samples was determined based on A.O.C.S. Official Method Ba10-65. Glucosinolate content of the samples was determined based on theMethod of the Canadian Grain Commission, Grain Research Laboratory(Daun, J. K. and McGregor, D. I., Glucosinolate Analysis of Rapeseed(Canola), Dec. 15, 1981). Solvent residues were determined using GC/MStechniques based on a modified method of A.O.C.S. Official Method, Ba13-87.

Example 1(a) Effect of Heat Treatment on Canola Seed (Brassica juncea)at Temperatures Between 75° C.-95° C.

Seven samples containing about 4 kg of canola seed (28 kg in total) wereadjusted from an original moisture content of about 6.25% to about 11%by adding water to the canola seed in a plastic pail with manualagitation for a few minutes. The canola seed in the pails was thencovered and tempered overnight in the laboratory.

After the canola seed had been tempered overnight, six samplescontaining about 4 kg of the tempered seed (about 24 kg in total) weresubjected to individual heat treatments with a combination of hightemperatures and short residence times using a lab scale as listed inTable 1. For control, a control sample (about 4 kg) of canola seed washeated in a microwave oven for 2 minutes (heat to 85-95° C.). The canolaseed was then covered with an aluminum foil and heated at 95° C. in aforced air oven for 30 minutes (Table 1).

After heat treatment, seven samples (about 4 kg each) of the heattreated canola seeds were flaked using a lab flaking mill and thenpressed, resulting in pressed oils and pressed protein cakes. Thepressed oils were analyzed for sulfur and free fatty acid (FFA)contents. The pressed cakes were stored in a freezer.

Seven samples (about 1 kg each) of the pressed cakes from the six heattreatment trials and one control were extracted using a solvent mixtureof butane and R-134a (1,1,1,2-tetrafluoroethane) to produce extractedoils and defatted canola meals. The press cake was loaded in a columnand the solvent mixture under 300 PSI pressure was flowed through thepress cake to fluidize the press cake particles. The oil was extractedfrom the cake at 50° C. The solvent mixture with oil in a liquid formwas pumped to a low pressure zone and the pressure was released. Thesolvent mixture turns into gas while the oil remains in a liquid statefor the separation of oil from the solvent mixture. The defatted canolameals were analyzed for protein dispersibility index (PDI), the resultsof which are shown in Table 3. The extracted oil samples were analyzedfor sulfur, phosphorus and FFA contents, the results of which are shownin Tables 4-6.

The remaining pressed cakes were extracted with methyl pentane for fivehours using a lab Soxhlet system. Approximately 6-8 L of fresh methylpentane were required for each extraction lot. The extracted oil wasrecovered by evaporation and desolventization to remove the solvent fromthe miscella under vacuum at 60° C. The extracted oil was analyzed forsulfur, phosphorus and FFA contents. The methyl pentane extracted mealswere desolventized in a laboratory fume hood for three days at roomtemperature. The moisture and oil contents of the pressed cake are shownin Table 7.

Example 1(b) Effect of Heat Treatment on Canola Seed (Brassica juncea)at Temperatures Between 100° C.-130° C.

Five samples containing about 4 kg (about 20 kg in total) of canola seedwere adjusted from an original moisture content of about 6.25% to about11% by adding water to the canola seed in a plastic pail with manualagitation for a few minutes. The canola seed in the pails was thencovered and tempered overnight in the laboratory.

After the canola seed had been tempered overnight, five samplescontaining about 4 kg of the tempered seed (about 20 kg in total) weresubjected to individual heat treatments with a combination of hightemperatures and short residence times using a lab scale as listed inTable 2. After heat treatment, the five samples (about 4 kg each) of theheat treated canola seeds were flaked using a lab flaking mill, and thenpressed. The pressed oils were analyzed for sulfur, phosphorus and FFAcontents. The pressed cakes were stored in a freezer.

Five samples (about 1.5 kg each) of the pressed cakes from the five heattreatment trials were extracted using a solvent mixture of butane andR-134a (1,1,1,2-tetrafluoroethane) to produce extracted oils anddefatted canola meals. The extracted oils were analyzed for sulfur andFFA contents. The defatted canola meals were analyzed for proteindispersibility index (PDI).

Discussion

In the heat treatment process, rapid heating makes it possible to exposethe canola seed to an increased temperature very quickly and thus toinactivate the enzymes (e.g. myosinase, lipase, phospholipase, etc.)This is a more economical way for consistent inactivation of enzymeswithout loss of lysine or other heat sensitive amino acids.

As shown in Table 3, the increase in the heat treatment temperature from75° C. to 100° C. resulted in the gradual decrease in the PDI of thedefatted meal. The decrease in PDI of the defatted meal accelerated whenthe temperature was increased from 105° C. to 130° C. The sharp drop inPDI occurred when the temperature was above 110° C. Typically, thehigher the heat treatment temperature, the higher the percentage ofprotein molecules being denatured and thus the lower the PDI of thedefatted meal.

The sulphur content in the pressed oil from canola seed without heattreatment was 46.9 ppm, which decreased sharply to 21.5 ppm and 9.77 ppmwith heat treatment at 75° C. and 80° C. for 15 seconds, respectively.Heat treatment at higher temperatures from 80° C. to 130° C. did nothave any major effect on the sulphur content in the pressed oil (asshown in Table 4).

The sulphur in the butane/R134a extracted oil decreased from the levelof 303 ppm without heat treatment to 99.3 ppm at 75° C. and 101 ppm at80° C. The sulphur level showed continuous reduction with increase inthe temperature of heat treatment except at 85° C.

The sulphur content in the methyl pentane extracted crude oil decreasedcontinuously in relation to the increase in temperature from 222 ppm at75° C. to 34.5 ppm at 95° C. Methyl pentane extracted oil had highersulphur levels at 75° C. and 80° C., but lower at 85-95° C. as comparedwith butane/R134a extracted oils.

The sulphur content in the pressed oil, the butane/R134a and methylpentane extracted oils of the control samples were high. In the heattreatment of the control samples, the canola seed was covered using analuminum foil and heated at 95° C. in a forced air oven for 0.5 hour.Because the heat transfer efficiency is low, the temperature of the seedin the oven might have been lower than 95° C. even though the oventemperature was set at that temperature. Therefore, myrosinase was stillmostly active, causing the breakdown of glucosinolates and release ofthe sulphur into the pressed and extracted oils.

The free fatty acid in the pressed oil decreased slightly with theincrease in the heat treatment temperature from 75° C. to 95° C. (asshown in Table 5). A sharp drop in FFA occurred at 100° C. and FFAshowed little change from 100-130° C. The FFA in the butane/R134aextracted oil showed significant decrease with the increase intemperature from 75-100° C., however a further increase in temperaturegained little benefit for the reduction in FFA (Table 5). The FFA inmethyl pentane extracted oil also decreased with the increase intemperature from 75 to 95° C. The increase in heat treatment temperatureenhanced the degree of inactivation of lipase, which in return reducedthe hydrolysis of oil by lipase and thus reduced the FFA content.

The FFA content in the oil is mainly dependent on the quality of seed.Improper handling or storage can cause elevated levels of FFA.

The phosphorus content of butane/R134a extracted oil was very lowranging from 2.93 ppm at 75° C. to 22.8 ppm at 95° C. as listed in seenin Table 6. The phosphorus content of the pressed oil was also low atheat treatment temperatures of 100, 105, 110, and 130° C. The phosphoruscontent of pressed oil from the heat treatment of 120° C. was 117 ppm.

The selection of a heat treatment temperature is a compromise betweenthe opposing effects on oil quality, meal quality and economics.Accordingly, in an embodiment, a heat treatment temperature of 100° C.results in a reasonably high PDI, lower sulphur, FFA and phosphorus inpressed and butane/R134a extracted oils.

Heat treatment of canola seed above 80° C. reduced the sulphur contentin pressed oil to levels below 10 ppm. The pressed oil accounted forabout 50-60% of total crude oil from the crushing operation. The heattreatment of canola seed reduced the sulphur content of butane/R134a andmethyl pentane extracted oils substantially with an increase intemperature. The high sulphur in the extracted oil is related to highglucosinolates content in the canola seed. The canola seed (B. juncea)contained about 22.95 μmoles/g of glucosinolates on a dry weight basis.If canola seed with a glucosinolate content of 12 μmoles/g or lower isused, the sulphur content in the extracted oil can be reduced furtherusing the same heat treatment condition.

For a heat treatment of 100° C. for 15 seconds, the phosphorus contentin the pressed and butane/R134a extracted oils was below 50 ppm.

Example 2 Protein Concentrate of about 65% Protein (a) Defatted Meal

Approximately 4 kg of canola seed (B. juncea) was adjusted from theoriginal 6.25% moisture to 11% moisture by adding water to canola seedin a plastic pail with manual agitation for a few minutes. The canolaseed in the pail was then covered and tempered overnight in thelaboratory. The tempered canola seed was then heat treated at 100° C.for 15 seconds.

After heat treatment, the canola seed was flaked using a lab flakingmill and then pressed. The pressed cake was stored in a freezer beforesolvent extraction. The pressed oil was recovered and stored in afreezer. The pressed cake was extracted with 6-8 liters of methylpentane at about 58-67° C. for 5 hours using a lab scale Soxhlet system.The extracted oil was recovered by evaporation and desolventization toremove the solvent from the miscella under vacuum at 60° C. Theextracted oil was stored in a freezer. The methyl pentane extracted mealor defatted meal was desolventized in a laboratory fume hood for threedays at ambient temperature. Approximately 2 kg of defatted meal wasproduced and stored at ambient temperature before further evaluation.

(b) Protein Enriched Meal

Approximately 2 kg of defatted meal was ground using a coffee grinderfor 15-20 seconds. The ground meal was screened through a 60 US meshscreen. Approximately 0.94 kg of fine meal (protein-enriched meal) and1.06 kg of coarse meal (fiber enriched meal) were obtained.

(c) 65% Protein Concentrate

Approximately 0.94 kg of protein-enriched meal was extracted by mixingwith 5.64 kg of 65% (v/v) ethanol at ambient temperature for 1 hour. Themixture was centrifuged at 4,000 g force for 15 minutes to separate theliquid sugar extract from the protein solids using a lab centrifuge. Thesugar extracts were combined together and concentrated using a lab BuchiRotavapor at 80° C., which was followed by freeze drying of theconcentrated sugar extract using a lab freeze dryer. The washedprotein-enriched meal was desolventized in a lab fume hood, which wasfollowed by drying in a lab forced air oven. Approximately 0.67 kg ofprotein concentrate containing 65% protein on a dry weight basis and0.21 kg of dried sugar fraction were produced, respectively. Theanalysis of the defatted meal, protein-enriched meal and 65% proteinconcentrate are shown in Table 8.

Example 3 Protein Concentrate of about 70% Protein (a) Ethanol Washingand Screening

The process for preparation of the protein-enriched meal was the same asin Example 2 except for (1) canola seed was cooked at 80° C. for 25minutes before pressing, and (2) the defatted meal was milled using adisc mill before screening through a 60 US mesh screen as describedbelow.

Approximately 1 kg of protein-enriched meal was mixed under homogeneousagitation with 6 kg of 80% (v/v) ethanol at 50° C.±5° C. for 1 hour,which was followed by screening the mixture through a 40 mesh US screento remove fiber. The screened mixture was centrifuged at 4,000 g forceusing a lab centrifuge for 15 minutes to separate the sugar extract fromthe protein solids. The protein-solids were mixed under homogeneousagitation with 6 kg of 80% (v/v) ethanol at 50° C.±5° C. for 0.5 hour.The washed protein solids was separated from the sugar extract bycentrifugation at 4,000 g force for 0.5 hour. The protein solids wereagain washed 6 kg of 80% (v/v) ethanol for at 50° C.±5° C. 0.5 hour,which was followed by centrifugation at 4,000 g force for 15 minutes.Finally the washed protein solids were dried to give a proteinconcentrate containing 70% protein on a dry weight basis. The ethanolwas recovered from the combined sugar extract through evaporation undervacuum at 80° C. using a lab Buchi Rotavapor. The concentrated sugarextract was spray dried into a dried sugar sample.

Example 4 Canola Protein Concentrate Having About 65-70% Protein Content

Three samples of a protein concentrate from Brassica juncea wereprepared in the following manners (the processing conditions for Samples1-3 are compared in Table 13):

(1) Sample 1—Moisture Adjustment

-   -   Approximately 2,919 kg of canola seed was adjusted from the        original about 6.25% moisture content to about 11% moisture by        adding 54 kg of water to the canola seed under mixing. The        moisture adjustment and mixing were executed as 14 batches due        to the capacity constraint of the Ribbon Blender (Table 9).        After the moisture adjustment, the canola seed was stored in        bins, covered and tempered overnight before pressing.

Pressing

-   -   The tempered canola seed was divided into two portions, (i)        300.5 kg of seed for pressing trial without flaking and (ii) the        remainder of the tempered seed (2,676 kg) for flaking and        pressing.    -   Approximately 300.5 kg of tempered seed was heat treated using a        two-tray cooker. The temperature of the top tray was 50-72° C.,        while the temperature for the bottom tray was 75-96° C. The        resident time for top and bottom trays was 20 minutes,        respectively. After heat treatment, the seed was fed into the        press and was pressed to produce 181.6 kg of press cake (Sample        1a). Press cake is a term that is synonymous with seed cake.    -   Approximately 2,676 kg of tempered seed was flaked to produce        flaked canola seed with an average thickness of 0.3±0.1 mm using        a flaking mill. The flaked canola seed was heat treated using a        two-tray cooker. The temperature for the top tray was 50-72° C.,        while the temperature for the bottom tray was 75-96° C. The        resident time for the top and bottom trays was 20 minutes,        respectively. After heat treatment, the flaked seed was fed into        the press and was pressed to produce 1,566 kg of press cake        (Sample 1b). Approximately 945 kg of press oil was produced from        the pressing trials of non-flaked and flaked seeds.        Approximately 42.9 kg of fine particles (foots) was produced in        the pressing trials. Approximately 85.3 kg of canola seed was        lost as floor sweeps, which are waste materials that drop on the        floor.

Solvent Extraction

-   -   Approximately (i) 181.6 kg and (ii) 1,566 kg of press cakes from        non-flaked and flaked canola seeds were extracted using a        solvent mixture of butane/R124a to produce extracted (defatted)        canola meals from the non-flaked press cake (Sample 1c) and the        flaked press cake (Sample 1d), in addition to extracted oils.        The solvent extraction of the press cakes was conducted at        50° C. for 1.5 hours.    -   As shown in Tables 10, 11 and 14, the press cake (Sample 1a)        from the non-flaking trial contained a high crude oil content of        26.81-32.37% on a dry weight basis.

Milling and Screening

-   -   Approximately 1,231 kg of extracted (defatted) meal (Sample 1d)        was produced from 1,566 kg of flaked press cake through solvent        extraction at 50° C. for 1.5 hours using a solvent mixture of        butane and R134a. The extracted meal was milled using a disc        mill equipped with #8114 stationary and rotating plates (The        Bauer Bros. Co., Springfield, Ohio, U.S.A.) at 0.02″ gap, 2340        rpm rotational speed and 200 kg/hr throughput. Only one pass        through the disc mill was conducted. Approximately 1,142 kg of        milled canola meal was produced. Approximately 88.9 kg of        material was lost in the milling operation with a recovery yield        of 92.78%. The milled canola meal was screened through a 43-45        US mesh screen using the Rotex® Vibratory Screen (from Rotex®,        Ohio, USA) at a feed rate of 200 kg/hr. Only one pass through        the screen was conducted. Approximately 423.66 kg of protein        enriched meal (fine fraction) and 717.00 kg of fiber enriched        meal (coarse fraction) were produced, respectively.        Approximately 1.64 kg of material was lost in the screening        operation with a recovery yield of 99.86%. After screening,        37.14% of the total material was protein enriched meal (Sample        1e) and 62.86% was fiber enriched meal (Sample 1f),        respectively, as seen in Table 12.

Preparation of Protein Concentrate from Protein Enriched Meal

-   -   Approximately 412 kg of protein enriched meal containing 6.90%        moisture and 53.92% protein (dwb) was mixed with about 2,400 kg        of 80% ethanol (v/v) in two 2600 L stainless steel tanks under        homogeneous agitation at room temperature for 1 hour. After        extraction, the protein slurry was centrifuged continuously        using a decanter centrifuge (Model CA220-21-33, Westfalia®        Separator, GEA Westfalia Separator® Inc., Northvale, N.J., USA)        to separate insoluble protein solids from the sugar extract. The        protein solids were mixed with 2,400 kg of 80% ethanol (v/v)        under homogeneous agitation at room temperature for 1 hour,        which was followed by centrifugation of the protein slurry using        the decanter to separate the washed protein solids from the        washing sugar extract. Finally, the washed protein solids were        mixed with 2,400 kg of 80% ethanol (v/v) under homogeneous        agitation at room temperature for 1 hour. The protein slurry was        centrifuged using the decanter to separate the final washed        protein solids from the washing sugar extract. The final washed        protein solids were desolventized and dried at 54±3° C. for 18        hours in a Littleford® vacuum dryer (Littleford Day®, Inc.,        Florence, Ky., USA) until the moisture content of the dried        solids reached 5±1%. The desolventized and dried protein solids        were milled using a Fitz mill fitted with a 0.033″ screen (The        Fitzpatrick Co., Elmhurst, Ill., U.S.A.). The milled protein        solids were screened using a Rotex Vibratory Screen (Model 111        A-MS/MS, Rotex Inc., Cincinnati, Ohio, U.S.A.) fitted with a        43-45 US mesh screen (POS #54 screen). Approximately 248.3 kg of        protein concentrate containing (Sample 1g) 65.80% protein (dwb)        and 5.51% moisture was produced.

(2) Sample 2—Preparation of Defatted Meal

-   -   Approximately 4.5 kg of extracted (defatted) canola meal (Sample        2a) was produced from non-flaked press cake through extraction        using a solvent mixture of butane and R134a at 50° C. for 2        hours. The non-flaked press cake was produced from canola seed        (B. juncea) by heat treatment of canola seed at 80° C. for 0.5        hour before pressing in a French Oil Machinery press.

Milling and Screening

Approximately 3.5 kg the defatted meal (Sample 2a) was milled for 1minute using a lab Waring® Blender, which was followed by manualscreening using a 45 US mesh Rotex screen to generate a protein fraction(fine fraction) and a coarse fraction. The coarse fraction was re-milledin the lab Warring Blender for 1 minute. This was followed by manualscreening using the 45 US mesh Rotex screen to generate the 2^(nd)protein fraction and a coarse fraction. Finally, the coarse fraction wasmilled in the Warring Blender for 1 minute and the milled material wasmanually screened using the 45 US mesh Rotex screen to generate the3^(rd) protein fraction and the fiber enriched meal. Approximately, 1.5kg of combined 1^(st), 2^(nd) and 3^(rd) protein fractions and 2 kg offiber enriched meal were produced, respectively. Therefore, 42.85% ofthe total material was the protein enriched meal (Sample 2b) and 57.15%was the fiber enriched meal (Sample 2c), as seen in Table 12.

Preparation of Protein Concentrate from Protein Enriched Meal

-   -   Approximately 1.5 kg of protein enriched meal containing 6.16%        moisture and 54.77% protein (dwb) was mixed with 9 kg of 80%        ethanol (v/v) in a stainless steel pot under homogeneous        agitation using an over head stirrer at room temperature for 1        hour. After extraction the slurry was centrifuged batch wise at        4,414 g (4,000 rpm) for 10 minutes to separate insoluble protein        solids from the sugar extract. For a second extraction, the        protein solids were mixed with 9 kg of 80% ethanol (v/v) under        homogeneous agitation at room temperature for 1 hour, which was        followed by centrifugation of the protein slurry at 4,414 g        (4,000 rpm) for 10 minutes to separate the washed protein solids        from the washing sugar extract. Finally, the washed protein        solids were extracted for a 3^(rd) time with 9 kg of 80% ethanol        (v/v) under homogeneous agitation at room temperature for 1        hour. The protein slurry was centrifuged at 4,414 g (4,000 rpm)        for 10 minutes to separate the final washed protein solids from        the washing sugar extract. The final washed protein solids were        desolventized and dried in a lab fume hood for over 3 days,        which was followed by drying in a forced air oven at 50° C. for        15 hours to reduce the ethanol residue. The desolventized and        dried protein solids were milled twice using a lab pin mill.        Approximately 1.1 kg of protein concentrate (Sample 2d)        containing 68.69% protein (dwb) and 5.52% moisture was produced.

(3) Sample 3—Preparation of Defatted Meal

-   -   Approximately 13.1 kg of defatted canola meal (Sample 3a) was        produced from non-flaked press cake through extraction using a        solvent mixture of butane and R134a at 50° C. for 1.5 hours. The        non-flaked press cake was produced from canola seed (B. juncea)        by heat treatment of canola seed at 80° C. for 0.5 hour before        pressing in a French Oil Machinery press.

Milling and Screening

-   -   Approximately 13.1 kg of the defatted meal (Sample 3a) was        milled using a disc mill equipped with #8114 stationary and        rotating plates (The Bauer Bros. Co., Springfield, Ohio, U.S.A.)        at 0.02″ gap and a speed of 1150 rpm for the rotating plate. The        milled meal was screened using a Rotex Vibratory Screen (Model        111 A-MS/MS, Rotex Inc., Cincinnati, Ohio, U.S.A.) fitted with a        43-45 US mesh screen (POS #54 screen) to generate 4.1 kg of        protein enriched meal (fine fraction) and 8.8 kg of coarse        fraction. The coarse fraction was fed to the disc mill at 0.015″        gap stationary and rotating plates of #8114 and a speed of 1150        rpm for the rotating plate. The milled coarse fraction was        screened using a Rotex Vibratory Screen fitted with a 43-45 US        mesh screen (POS #54 screen) to generate 1.1 kg of protein        enriched meal (fine fraction) and 7.7 kg of fiber enriched meal.        After screening, 40.31% of the total material was protein        enriched meal (Sample 3b) while 59.69% was fiber enriched meal        (Sample 3c) (see Table 12).

Preparation of Protein Concentrate from Protein Enriched Meal

-   -   Approximately 3.9 kg of protein enriched meal containing 6.5%        moisture and 52.62% protein (dwb) was mixed with 23.4 kg of 80%        ethanol (v/v) in a stainless steel pot under homogeneous        agitation using an over head stirrer at room temperature for 1        hour. After extraction the slurry was centrifuged batch wise at        4,414 g (4,000 rpm) for 10 minutes to separate the insoluble        protein solids from the sugar extract. The protein solids were        mixed with 23.4 kg of 80% ethanol (v/v) under homogeneous        agitation at room temperature for 1 hour, which was followed by        centrifugation of the protein slurry at 4,414 g (4,000 rpm) for        10 minutes to separate washed protein solids from the washing        sugar extract. Finally, the washed protein solids were extracted        for a 3^(rd) time with 23.4 kg of 80% ethanol (v/v) under        homogeneous agitation at room temperature for 1 hour. The        protein slurry was centrifuged at 4,414 g (4,000 rpm) for 10        minutes to separate the final washed protein solids from the        washing sugar extract. The final washed protein solids were        desolventized and dried in a lab fume hood for over 3 days. The        desolventized and dried protein solids were milled using a lab        hammer milled fitted with a 14 US mesh screen, which was        followed by further milling through a lab pin mill twice. The        milled protein solids were manually screened using a lab Rotex        screen fitted with a 60 US mesh screen to obtain 2.38 kg of        protein concentrate (Sample 3d) containing 69.6% protein (dwb)        and 0.25 kg of coarse fraction containing 59.1% protein (dwb).        The protein concentrate was dried in a forced air oven at 50° C.        for 15 hours to reduce the ethanol residue.

Vacuum Drying of Samples 1-3

-   -   One kilogram samples of Samples 1c, 1d, 2a, 2d, 3a and 3d were        loaded into 6 metal trays, which were placed in a freeze dryer        (Model 50 SRC-6 Subliminator, Virtis Company, Gardiner, N.Y.).        Drying was started at 50° C. and a maximum vacuum attainable        (absolute pressure of 150-500 μHg) by the dryer. Drying was        continued at 50° C. for 15 hours. After drying, nitrogen was        injected into the dryer while vacuum was released slowly. The        samples were tested for solvent residues.

Discussion

The mass balance data for flaking and pressing trials for Samples 1a and1b are shown in Table 10 and FIG. 12, while the proximate analysisresults for the Samples are listed in Table 11. Further, the moistureand oil contents of the press cakes of Sample 1 are given in Tables 14and 15.

The average oil content in the flaked press cake (Sample 1b) ascalculated from the results in Table 15 is 15.18% (dwb). The averagemoisture content in the flaked press cake (Sample 1b) is 7.87%. The oilcontent in the starting canola seed is 44.39% (dwb) (Table 11).Moreover, 1,566 kg of flaked press cake (Sample 1b) contained 219 kg ofcrude oil, while the starting 2,676 kg of canola seed after the moistureadjustment contained 1,091 kg of crude oil (see FIG. 12). Approximately872 kg of crude oil or 79.93% of the total crude oil was pressed out ofthe flaked seed during the pressing operations.

The average oil content in the non-flaked press cake (Sample 1a) ascalculated from the results in Tables 10 and 11 was 29.83% (dwb). Theaverage moisture content in the non-flaked press cake (Sample 1a) was8.31% (Tables 11 & 14). Moreover, 181.6 kg of non-flaked press cakeSample 1) contained 49.7 kg of crude oil, while the 301 kg of startingcanola seed after the moisture adjustment contained 122.8 kg of crudeoil. Approximately 73.1 kg of crude oil or 59.52% of the total crude oilwas pressed out of the non-flaked seed during the pressing operation.

Non-flaked press cake (Sample 1a) contained much higher crude oilcontent than that of flaked press cake (Sample 1b). Higher ratio ofpress oil was obtained from the flaked seed than from the non-flakedseed in the pressing operation. After solvent extraction, defattedcanola meal (Sample 1c) from non-flaked press cake still contained ahigh oil content of 8.75%-12.73% (dwb) while defatted meal (Sample 1d)from flaked press cake contained less than 3.13% of crude oil (Tables 14& 16). Visual inspection of the non-flaked press cake showed that itcontained many intact seeds, making it difficult for oil extraction bythe solvent mixture of butane and R134a. Flaking would be required torupture the oil cells before pressing to obtain high ratio of press oilin the pressing operation and lower oil content in the solvent extractedmeal. Defatted meal (Sample 1d) from flaked press cake was used as thestarting material for the preparation of a protein concentrate. Defattedmeal from non-flaked press cake was not used for the preparation ofprotein concentrate due to its high oil content.

The fractions of protein enriched and fiber enriched meals (Samples 1eand 10 from milling and screening trials are shown in Table 12, whilethe results of the proximate analysis are given in Table 17. As seen inTable 12 for Sample 1e, approximately 42.33% to 57.23% of the totalmaterial was generated as protein enriched fraction and 42.76% to 57.66%as fiber enriched fraction (Sample 10. From the screening trial of thismilled juncea meal, approximately 37.14% was protein enriched meal while62.86% was fiber enriched meal.

As shown in Table 17, the protein content was increased from47.02-49.98% (dwb) in the extracted or defatted meals to 52.62-54.77%(dwb) in the protein enriched meals by the milling and screeningoperation (Samples 1d, 2a and 3a compared to Samples 1e, 2b and 3b). Thecrude fiber content was reduced from 8.28-9.79% (dwb) in the extractedmeals to 4.82-5.49% (dwb) in the protein enriched meals (Samples 1f, 2cand 3c compared to Samples 1e, 2b and 3b). A simple step of dry millingand screening generated a starting material with higher protein andlower fiber contents for protein concentrate preparation.

The mass balance flow charts for preparation of protein concentrates(Samples 1g, 2d and 3d) from protein enriched meals are shown in FIGS.13, 14 and 15. As seen in Table 17, the moisture content of proteinconcentrates was in the range of 5.32-5.52%, the protein content ofprotein concentrates (Samples 1g, 2d and 3d) was in the range of65.80-69.60% (dwb). The crude oil content of protein concentrates was inthe range of 0.02-0.41% (dwb) (Samples 1g, 2d and 3d), while the crudefiber content of protein concentrates was in the range of 6.37-7.16%(dwb). The yield of protein concentrates is listed in Table 18.Approximately 0.6-0.733 kg of protein concentrate containing65.80-69.60% protein (dwb) was produced from 1 kg of protein enrichedmeal containing 52.62-54.77% protein (dwb).

Protein concentrates from Samples 1g, 2d and 3d contained 65.80%, 68.69%and 69.60% protein (dwb). Protein concentrates contained 6.37-7.16%crude fiber on a dry weight basis (Table 17), which was higher than thecrude fiber content of around 3.8-4.5% for soy protein concentrate.

Ethanol extraction was effective to increase the protein content from52.62-54.77% (dwb) in the protein enriched meals to 65.8-69.6% (dwb) inthe protein concentrates (Samples 1g, 2d and 3d). Ethanol washing wasalso effective in reducing the crude oil content from 0.51-1.49% (dwb)in protein enriched meals to 0.02-0.41% (dwb) in the proteinconcentrates.

Sample 2d was analyzed for its components and the test results arelisted in Table 19. The amino acid profile Sample 2d is given in Table20. Samples 1d, 2a and 3a; 1f, 2c and 3c; and 1g, 2d and 3d wereanalyzed. Results are shown in Tables 21, 22 and 23 for the contents ofantinutritional factors such as glucosinolates, phytates and sinapines.

The glucosinolate and sinapine contents were reduced significantly byusing 80% ethanol washings when protein concentrate (Samples 1g, 2d and3d) was produced from Samples 1d, 2a and 3a (Tables 21-23).

The results of solvent residues analysis are listed in Table 24. Theresults of solvent residue analysis after desolventization and dryingare shown in Table 25.

Samples 1d, 1f, 2a, 2c, 3a and 3c contained high solvent residues ofbutane and R134a before vacuum drying. After vacuum drying, the solventresidues of had been reduced significantly. The residues of butane andR134a in Samples 1d, 1f, 2a and 2c were reduced to below the detentionlimit of 10 ppm respectively. After drying of Samples 2d and 3d at 50°C. for 15 hours in the forced air oven and drying of Sample 1g at 54±3°C. for 18 hour in the Littleford® vacuum dryer, they contained less than10 ppm of butane and less than 10 ppm of R134a.

In the pressing and extraction trials of Sample 1, non-flaked press cake(Sample 1a) contained much higher crude oil content than that of flakedpress cake (Sample 1b). After solvent extraction the defatted canolameal from non-flaked press cake (Sample 1c) contained a high oil contentof 8.75%-12.73% (dwb) while the defatted meal from flaked press cake(Sample 1d) contained less than 3.13% (dwb) residual crude oil. Visualinspection of the non-flaked press cake showed that it contained manyintact seeds, making it difficult for efficient oil extraction by thesolvent mixture of butane and R134a. Flaking would be required torupture the oil cells before pressing to increase the ratio of press oiland obtain a lower oil content in the solvent extracted meal.

Milling of Sample 1d using a disc mill went smoothly with a throughputof 200 kg per hour. 47.93% protein enriched (Sample 1d) and 52.07% fiberenriched meals (Sample 1f) were produced in lab screening trials of themilled extracted meal using a Rotex screen of 45 US mesh. In thesescreening trials, up to 57.23% protein enriched meal (Sample 1e) wasobtained. 37.14-40.31% protein enriched and 59.69-62.86% fiber enrichedmeals were produced from the screening of the milled extracted meals.The protein enriched meals (Samples 1e, 2b and 3b) contained52.62-54.77% protein on a dry weight basis.

Protein concentrates (Samples 1g, 2d and 3d) containing 65.80-69.60%protein on a dry weight basis were prepared from protein enriched mealssubjected to three 80% ethanol (v/v) washings. 60.27-73.33% recoveryyields for protein concentrates were obtained based on the weight ofstarting protein enriched meals. Antinutritional factors such asglucosinolates and sinapines were reduced dramatically by 80% ethanolwashings of protein enriched meals. Protein concentrates contained6.37-7.16% crude fiber on a dry weight basis, which was still higherthan the crude fiber content of around 3.8-4.5% for soy proteinconcentrate. A wet separation method was utilized to reduce the crudefiber content to 3.20-4.88% (dwb) in the canola protein concentrates(Samples 1g, 2d and 3d) using a decanter centrifuge to separate thefiber from insoluble and soluble proteins based on the difference indensity.

Samples 1d, 2s and 3a, and 1f, 2c and 3c contained high solvent residuesof butane and R134a before vacuum drying. After vacuum drying, thesolvent residues had been reduced significantly.

Example 5(a) Canola Protein Concentrate Having about 70% Protein Content(i) Screening and Aspiration of Canola Seed

Approximately 523.5 kg of canola seed (Brassica juncea) was screenedthrough a Rotex vibratory Screen (Model 111 A-MS/MS, Rotex Inc.,Cincinnati, Ohio, U.S.A.) fitted with a 10 US mesh screen to separatethe seed from large size of foreign materials. The screened canola seedwas fed to a Kice Aspirator (Kice Metal Products Company Inc., Wichita,Kans., USA) and aspirated into two fractions, the clean seed and thelight foreign materials. Approximately 21.8 kg of foreign materials and499 kg of clean seed were produced from the screening and aspirationoperations. The clean seed contained 8.12% moisture. A schematicflowchart for screening and aspiration of canola seed is shown in FIG.16.

(ii) Screw Pressing of Cleaned Canola Seed

Approximately 499 kg of the cleaned canola seed was flaked to produceflaked seed with an average thickness of 0.3±0.1 mm using a flaking mill(Model S28, Lauhoff Corporation, Detroit, U.S.A.). The flaked canolaseed was heat treated using a two tray cooker. The temperature for thetop tray was 52-59° C., while the temperature for the bottom tray was68-90° C. The resident time for the top and bottom trays was 20 minutes,respectively. After heat treatment, the flaked seed was fed into thepress and pressed to produce 278.9 kg of press cake and 138.1 kg ofpress oil.

(iii) Solvent Extraction of Press Cake

Approximately 278.9 kg of press cake was subjected to a solventextraction which was conducted at 50° C. for 1.5 hours using a solventmixture of butane and R134a. Approximately 201.4 kg of defatted(extracted) meal containing 47.0% protein on a dry weight basis wasproduced from 278.9 kg of press cake.

s(iv) Milling and Screening of Defatted Meal

The defatted meal (201.4 kg) was milled using a disc mill equipped with#8114 stationary and rotating plates (The Bauer Bros. Co., Springfield,Ohio, U.S.A.) at 0.02″ gap, 2340 rpm rotational speed and 100 kg/hthroughput. Only one pass through the disc mill was conducted. Aschematic flowchart for milling and screening of the defatted meal isshown in FIG. 17. Approximately 193 kg of milled defatted canola mealwas produced. Approximately 8.4 kg of material was lost in the millingoperation with a recovery yield of 95.83%.

The milled defatted canola meal was screened through a 45 US mesh screenusing the Rotex Vibratory Screen at a feed rate of 100 kg/hr. Only onepass through the screen was conducted. Approximately 76.85 kg of proteinenriched meal (fine fraction) and 114.8 kg of fiber-enriched meal(coarse fraction) were produced, respectively. Approximately 1.35 kg ofmaterial was lost in the screening operation with a recovery yield of99.30%. After screening, 40.1% of the total material was proteinenriched meal and 59.9% was fiber enriched meal, respectively.

(v) Wet Separation to Remove Fiber

Approximately 71.9 kg of protein enriched meal was mixed with 575 kg oftap water at a ratio of about 1 to 8 (by weight) under homogeneousagitation to form a protein slurry. The protein slurry was adjusted topH 8.9 by slow addition of 7.6 kg of 11.06% NaOH solution underhomogeneous agitation. This was followed by centrifugation at roomtemperature using a Bird Decanter Centrifuge (Bird 6″ Continuous BowlCentrifuge, Bird Machine Company of Canada, Saskatoon, Saskatchewan).The protein slurry was pumped through the Bird Decanter at ambienttemperature and a feed rate of 150 kg/h and it was operated at a bowlspeed of 1,500 rpm with a low pool depth to separate the coarse fibersolids from the soluble and insoluble protein fractions. Approximately161.9 kg of wet fiber solids containing 15.42% solids and 511.5 kg ofprotein slurry containing soluble and insoluble proteins at 8.26% solidswere produced, respectively. 161.9 kg of wet fiber solids was mixed with161.9 kg of water in a tank for 0.5 hour as a second extraction, whichwas followed by centrifugation at room temperature using the BirdDecanter at a bowl speed of 1,500 rpm and a feed rate of 160 kg/hr.Approximately 74.2 kg of washed wet fiber and 299 kg of protein slurrycontaining soluble and insoluble proteins were produced. Proteinslurries containing soluble and insoluble proteins from these twocentrifugations were combined and approximately 810.5 kg of the combinedprotein slurry was obtained. A schematic flowchart illustrating the wetseparation of fiber is shown in FIG. 18.

Discussion

The Bird Decanter can operated at a bowl speed of 1,000-5,000 rpm(100-2130 g) and a pool depth of 5 to 19 mm. A spin down of the proteinslurry sample in a centrifuge tube using a bench top centrifuge showedthree layers, liquid extract as the top layer, insoluble protein cake offine protein particles as the middle layer and the coarse fiber solidsas the bottom layer. The objective was to separate the top and middlelayers (the soluble protein extract and the insoluble fine proteinsolids) from the bottom layer (coarse fiber solids). The bird decanterwas operated at a low pool depth and a bowl speed of 1,000, 1,500,2,000, 2,500 and 3,000 rpm and the separation efficiency was evaluatedby spin down tests of the feed, the fiber fraction and the proteinslurry using the bench top centrifuge. Separation of the coarse fibersolids from the insoluble fine protein solids and the soluble proteinextract was obtained at a bowl speed of about 1,000 rpm to about 2,000rpm, optionally about 1,500 rpm (˜760 g) and a low pool depth.

(vi) Preparation of Protein Concentrate Containing 70% Protein

Approximately 8.7 kg of protein slurry containing soluble and insolubleproteins after the fiber removal using the Bird Decanter was mixed with8.6 kg of SDAG-13 denatured ethanol (containing 99% ethanol and 1% ethylacetate) for 0.5 hours at room temperature. This was followed bycentrifugation for 10 minutes using a lab centrifuge at 4,200 rpm toobtain 14.8 kg of a first sugar extract containing 1.42% solids and 2.5kg of a first wet protein solid fraction. The wet protein solid fraction(2.5 kg) was further mixed with 4.3 kg of SDAG-13 denatured ethanol for1 hour at room temperature. This was again followed by centrifugationfor 10 minutes using the lab centrifuge at 4,200 rpm to obtain 4.7 kg ofa second sugar extract and 2.1 kg of a second wet protein solidfraction. Finally, the wet protein solid fraction (2.1 kg) was mixedwith 4.3 kg of SDAG 13 denatured ethanol for 1 hour at room temperature,which was followed by centrifugation for 10 minutes using the labcentrifuge at 4,200 rpm to obtain 4.3 kg of a third sugar extract and2.1 kg of a third wet protein solid fraction. The wet protein solidswere dried in a lab forced air oven at 50° C. until the moisture contentwas about 6%. The dried protein solids were milled using a lab pin millto obtain the final protein concentrate containing 70.6% protein on adry weight basis. A schematic flowchart illustrating the preparation ofa protein concentrate containing 70.6% protein is shown in FIG. 19.

Example 5(b) Canola Protein Isolate

Approximately 770 kg of a protein slurry containing soluble andinsoluble proteins prepared in the same manner as in Example 5a(i)-(v)(including fiber removal using the Bird Decanter), was centrifuged usinga Westfalia® Decanter (Model CA 225-010, Centrico Inc., Northvale, N.J.,USA) at ambient temperature and a bowl speed of 5,200 rpm (3,300 g) toseparate the soluble protein extract from insoluble protein solids.Approximately 650 kg of a first protein extract containing solubleproteins and 120 kg of a first protein solid fraction were produced. Thefirst protein solid fraction was mixed with 360 kg of water at roomtemperature for 0.5 hour under homogeneous agitation, which was followedby centrifugation using the Westfalia® Decanter to obtain 368.5 kg of asecond protein extract containing soluble proteins and 91.3 kg of asecond protein solids fraction.

The first and second protein extracts were combined together and thecombined extract was centrifuged using a Westfalia® Disc StackCentrifuge (Model SA14-02-073, Centrico., Northvale, N.J., USA) atambient temperature and a bowl speed of 8,500 rpm (6,549 g) to removetrace insoluble solids in the soluble protein extract. Approximately978.5 kg of clarified protein extract and 21.9 kg of a third proteinsolids fraction were produced.

The clarified protein extract was adjusted to pH 7.0 by addition of 1.8kg of 11% NaOH solution, which was followed by concentration of theprotein extract in the feed tank from 978.5 kg to 140 kg at ambientusing a Millipore® Ultrafiltration Unit from Millipore®, Mass., USA. TheUltrafiltration Unit (UF) was fitted with three hollow fiber cartridgeswith a molecular weight cutoff of 10,000 daltons, with each cartridgecontaining 5 m² of membrane surface area. The protein extract was pumpedthrough the hollow fiber cartridges at a rate of 800-1000 kg/hr. Theretentate was recycled back to the feed tank and the permeate wascollected in another tank. The UF unit was operated at an inlet pressureof 25 psi maximum and a retentate back pressure of 15 psi maximum. Theflux rate or permeate rate was about 120 kg/hr initially and graduallydecreased to about 70 kg/hr and stabilized at that level for a period oftime before decreasing further. Back flushing was conducted to increasethe flux rate periodically. The ultrafiltration process continued untilthe amount of protein solution in the feed tank was equal to about 15%of its initial weight.

Approximately 60 kg of water was added into the feed tank anddiafiltration was conducted at ambient temperature using the same UFunit fitted with the same three hollow fiber cartridges. The originalvolume of protein solution in the feed tank was held constant by addingwater to make up for the removed permeate. The retentate was recycledback to the feed tank. The amount of water added to maintain theoriginal volume of protein solution was about 2.8 times the originalvolume of protein solution or 560 kg.

Approximately 311 kg of purified protein extract was obtained from theultrafiltration and diafiltration process. The purified protein extractwas heated to 40±10° C. using a heat exchanger prior to being fed to aKomline Sanderson® spray dryer (Komline Sanderson® Ltd., Brampton,Ontario, Canada) by pumping at a feed rate of 150-165 kg per hour. Thespray drying operation was conducted at an inlet air temperature of185±5° C. and an outlet air temperature of 85±5° C. Approximately 7.85kg of spray dried protein isolate was produced. A schematic flowchartillustrating the preparation of a canola protein isolate is shown inFIG. 20.

Using gel permeation chromatography, the canola protein isolate had amolecular weight profile wherein the isolate contains 64.7% of theproteins have a molecular weight of 70 kDa, 26.2% at 12 kDa and 9.1% at<10 kDa.

Example 5(c) Preparation of Hydrolyzed Protein Concentrates

Approximately 91.3 kg of the second protein solid fraction and 21.9 kgof the third protein solid fraction (obtained from Example 5(b)) wereadded to 260 kg of water in a tank, resulting in a slurry of about 5%solids in a 2000 L scraped surface tank. This was followed by pHadjustment to 8.3±0.1 using 8% NaOH solution. Approximately 200 g of afirst protease (Alcalase® 2.4 L FG) was added to the slurry. The slurrywas then heated to 60±2° C. and held at temperature for 4 hours. Theslurry was cooled down to 50±2° C. and 200 g of a second protease(Flavourzyme®) was added to the slurry, which was followed by holding at50±2° C. for 4 hours. The slurry was centrifuged using the Westfalia®Decanter at 3300×g to separate the hydrolyzed protein extract from theinsoluble fiber fraction. The insoluble fiber was washed further with100 kg of filtered tap water, which was again followed by centrifugationat 3300×g to separate the washed protein extract from the washed fibersolids using the Westfalia® Decanter. A sample of the washed proteinextract was taken to analyze the protein content.

Hydrolyzed protein concentrates were also produced from the combinedprotein slurry after fiber removal using the Bird Decanter (Example5a(i)-(v)). Approximately 7.48 kg of protein slurry containing solubleand insoluble proteins was adjusted from pH 8.3 to pH 7.0 by addition of25% phosphoric acid. After pH adjustment, the protein slurry wascentrifuged at 4,000 RPM to separate the soluble protein extract fromthe insoluble solids. Approximately 1.15 kg of insoluble solids wasmixed with 3.4 kg of water, which was followed by centrifugation at4,000 RPM to separate the first washing extract from the first washedsolids fraction. Approximately 1.07 kg of the first washed solids wasmixed with 3.4 kg of water. This was followed by centrifugation atambient temperature at 4,000 RPM to separate the second washing extractfrom the second washed solids fraction.

Approximately 1.07 kg of the second washed solids fraction was mixedwith 2.2 kg of water to obtain a slurry, which was followed by pHadjustment to 8.2 with the addition of 1 M NaOH solution. Approximately1.16 g of a first proteinase (Alcalase® 2.4 L FG) was added to theslurry. The slurry was heated to about 62° C. and held at thistemperature for 4 hours. The slurry was cooled down to about 50° C. andapproximately 1.16 g of a second proteinase (Flavourzyme®) was added tothe slurry, which was followed by holding at 50° C. for 4 hours.Finally, the slurry was centrifuged at 4,000 rpm for 10 minutes toseparate the hydrolyzed protein extract from the insoluble fiberfraction. The hydrolyzed protein extract was spray dried into hydrolyzedprotein concentrate using a lab spray dryer. A schematic flowchartillustrating the preparation of hydrolyzed protein extract is shown inFIGS. 20 and 21.

Using gel permeation chromatography, the hydrolyzed protein had amolecular weight profile wherein 63.3% of the hydrolyzed protein has anapproximate molecular weight of 9,500 daltons while 16.4% hydrolyzedprotein has approximate molecular weight of 7,000 daltons. The remaining20.3% of the hydrolyzed protein has an approximate molecular weight ofless than 5,000 daltons.

Discussion

The results of the proximate analysis for canola seed, press cake,defatted meal, protein enriched meal, fiber enriched meal, proteinconcentrate, hydrolyzed protein concentrate and protein isolate areshown in Table 26.

As shown in Table 26, dry separation by milling using a disc mill andscreening using a vibratory screen of 45 US mesh increased the proteincontent from 47% in the extracted meal to 52% in the protein enrichedmeal on a dry weight basis. The fiber content was reduced from 7.75% inthe extracted meal to 5.53% in the protein enriched meal by dryseparation. Wet separation to remove fiber using the Bird Decanter andto remove sugar compounds by the ethanol extraction process furtherincreased the protein content from 52% in the protein enriched meal to70.6% in the protein concentrate. The fiber content was reduced from5.53% in the protein enriched meal to 4.88% in the protein concentrateby wet separation using the bird decanter.

As shown in Table 27, wet separation to remove fiber by the BirdDecanter decreased the crude fiber content from 5.53% in the proteinenriched meal (see Table 26) to 3.20% in the protein slurry (see Table27) after the first fiber removal. The fiber fraction after the firstfiber separation contained about 10.2% crude fiber. The fiber fractionwas washed with water at a ratio of 1 to 1 by weight, which was followedby centrifugation using the Bird Decanter to separate the washed fiberfraction from the washing protein slurry. The washed fiber fractioncontained 12.7% crude fiber. The fiber washing step was able to increasethe crude fiber content in the fiber fraction from 10.2% to 12.7% on adry weight basis. More importantly, the washing step significantlyreduced the weight of fiber fraction from 161.9 kg to 74.2 kg or about54% and thus increased the protein recovery yield in the final proteinconcentrate. The washed fiber fraction contained 11.34 kg of total drysolids (74.2 kg×15.33% solids=11.34 kg) or 16.91% of starting proteinenriched meal on a dry weight basis.

After dry separation by screening, the protein enriched meal produced bythis process still contained a high crude fiber content of 5.53% on adry weight basis (see Table 26). A wet separation process was employedto separate and remove fiber from the soluble protein extract and theinsoluble protein particles taking advantage of the difference indensity and particle size between the fiber and insoluble proteinparticles.

Several spin down tests were performed on a protein slurry sample of10.4% solids in a centrifuge tube in the laboratory using a labcentrifuge, three layers of top liquid layer, the middle proteinparticle layer and the bottom fiber layer were obtained in the tube. Thefiber particles settled faster than the smaller insoluble proteinparticles. The settling rate was dependent on the g force—the higher theg force, the higher the settling rate. If the decanter centrifuge is runat a full bowl speed of 5,000 rpm or 3000 g force, both fiber andinsoluble protein particles settle and would be separated from theliquid extract and be removed by the decanter as the combined insolublesolids. If the decanter is run at a lower bowl speed of 1,500 rpm or alower g force of 750 g, the large fiber particles settle, but the fineprotein particles have not yet had sufficient time to settle, thereforethe fiber particles can be separated from the insoluble proteinparticles and the protein extract. The separation of fiber from proteinparticles is mainly caused by the difference in density between theinsoluble fiber and protein particles. A schematic flowchart for thefiber removal process is illustrated in FIG. 22.

The protein enriched meal was mixed with water at a ratio of 1 to 8 byweight and pH was adjusted to 8.9. After 1 hour of hold time underagitation at room temperature, the protein slurry was centrifuged at alow bowl speed of 1,500 RPM (˜750 g force) using the Bird Decanter.Larger fiber particles with higher density were separated from smallerinsoluble protein particles with lower density as well as solubleprotein solution. The fiber fraction was washed with water at a ratio of1 to 1, which was followed by centrifugation at 1,500 RPM using the BirdDecanter to separate the large fiber particles with higher density fromthe insoluble smaller protein particles with lower density as well asprotein extract. In an embodiment, the efficiency of a wet fiberseparation is affected by viscosity and density of the liquid medium.The soluble protein extract would be cycled and re-used to increase thesoluble solid content in order increase the density and viscosity of theliquid medium. This also helps to reduce the volume of water usage.

The results of the amino acid profiles for the canola proteinconcentrates and isolate on a dry weight basis are shown in Table 28. Inaddition, a comparison of amino acid profiles for the canola proteinconcentrate, canola protein isolate and commercially available soy andpea protein isolates is shown in Tables 29 and 30.

From the amino acid profiles as shown in Tables 28, 29 and 30, canolaprotein compares favorably to that of soy protein or pea protein. Canolaprotein is of high nutritional quality and capable of providing adequateamounts of all essential amino acids. Canola protein contains muchhigher sulphur containing amino acids such as methionine and cystinethan soy and pea proteins. Canola protein contains 48-72% highermethionine than soy protein and 70-97% higher methionine than peaprotein. Usually, cereals tend to be low in lysine but adequate in thesulphur containing amino acid methionine. Legumes are adequate in lysinebut low in methionine. Canola protein is unique in that it contains bothadequate lysine and sulphur containing amino acid methionine. Therefore,it exhibits a better amino acid balance than cereal proteins and legumeproteins (such as pea protein and soy protein). Canola protein hasexcellent nutritional quality and can be used in applications such asbaby formula and foods required for good nutrition.

From the essential amino acid profiles as shown in Table 30, canolaprotein is very rich in the muscle building essential amino acids suchas valine, methionine, leucine and isoleucine. It also contains a muchhigher content of the essential amino acid threonine, which is importantfor brain activity. Canola protein concentrate and isolate may besuitable ingredients for sports nutritional supplements.

With respect to the molecular weight and characterization of the canolaprotein concentrate, the concentrate obtained in Example 5(a) containedthree major subunits as listed below:

(a) 10,000-12,000 dalton molecular weight

(b) 15,000-20,000 dalton molecular weight

(c) 25,000-37,000 dalton molecular weight

The results obtained using a technique of Gel Permeation Chromatographyshow that canola protein isolate contains 64.7% of the proteins atmolecular weight of 70 kDa, 26.2% at 12 kDa and 9.1% at <10 kDa.

With respect to the functional properties of the canola protein isolate,the emulsifying and foaming properties of the canola protein isolate(obtained in Example 5(b)) as compared to soy and pea protein isolatesare shown in Table 31. As seen in Table 31, the canola protein isolateof the present disclosure has much better foaming capacity than soy andpea protein isolates at pH 7.0 and a protein concentration of 0.5%. AtpH 7 and concentration of 1.0%, canola protein isolate has slightlylower foaming capacity than soy protein isolate, but much higher foamingcapacity than pea protein isolate. The canola protein isolate has a muchbetter foam stability than soy and pea protein isolates. Further, thecanola protein isolate has similar emulsifying properties as compared tosoy and pea protein isolates at pH 7 and concentrations of 0.5% and1.0%, and also has similar emulsion stability at pH 7 and concentrationsof 0.5% and 1.0%.

The foaming capacity of a protein is characterized by whipping thedissolved protein at 0.5% protein content with a milk foamer(Aeroflott™) at 20° C. for 1 minute. Foam height was determined in a 100ml scaled cylinder for 1 hour. Additionally, the protein solution at0.5% protein was heated at 60° C. for 15 minutes and then cooled to 20°C. before foam test

The emulsifying capacity of a protein is defined as the maximum amountof oil which can be emulsified with a defined amount of protein forminga stable emulsion. The higher the emulsifying capacity, the higher theeffectiveness of the protein substance. The emulsifying capacity ismeasured by using the following emulsifying conditions:

(1) measuring temperature at 20° C.

(2) protein concentration at 0.5%

(3) stepwise addition of coloured plant oil (starting point at 50%)

(4) Emulsification using Ultra-Turrax (13,000 min⁻¹; 60 s)

(5) Evaluation of oil separation 30 minutes after emulsification.

As shown in Table 32, the emulsifying results of a 0.5% canola proteinisolate solution were very good as compared to a 5% egg yolk solution.Further, as described in Table 32, the canola protein isolate possessesthe functional property of gel formation and water immobilization, andtherefore, would act as a stabilizer. The results of gel firmness forcanola protein isolate are good and comparable to other vegetableproteins. The results of water immobilization of canola protein isolategels are good as compared to that of whey protein isolate gels, which isan important parameter for stability and shelf-life of a final productcontaining canola protein isolate.

Because of its emulsifying and foaming properties, in an embodiment, thecanola protein isolate is a suitable protein and functional ingredientin food applications that require good emulsifying and foaming capacityand stability such as in cakes, coffee toppings, and specialty coffeedrinks, crèmes, dressings and pastes. In another embodiment, the canolaprotein isolate is used for laundry and cosmetic products that requiregood foaming capacity and stability such as in laundry detergents, bathsoaps, conditioning shampoos, and cream hand and skin cleansers. In afurther embodiment, the canola protein isolate is used for soups, saladdressings, sausages, bologna and other comminuted and emulsified meatproducts that require good emulsifying capacity.

As seen in Table 33, the solubility of the canola protein isolate, inaddition to the solubility for pea and soy protein isolates is shown.The results show that 99.81% of the crude protein canola isolate crudeis soluble. The test results demonstrate that the canola protein isolateof the present disclosure has 99.81% soluble crude protein as comparedto 25.21% and 18.85% soluble crude protein for soy and pea proteinisolates, respectively. Accordingly, in an embodiment, the canolaprotein isolate is a suitable protein ingredient for nutritionalbeverages such as protein fortified soft drinks, fruit juices, sportsdrinks and high protein drinks. In another embodiment, it is also usefulfor healthy food applications to improve absorption and digestibility.

As shown in Table 34, the concentrations of antinutritional factors inthe canola protein isolate obtained in Example 5(b) are illustrated.Accordingly, the canola protein isolate contains very low levels oftotal glucosinolates, phytic acid and allyl isothiocyanate.

The results of glucosinolates in the canola seed, the canola press cake,the defatted meal, the protein and fiber enriched meals, the proteinconcentrates and isolate are shown in Table 35. The content of totalaliphatic glucosinolates in seed, press cake, extracted meal, proteinand fiber enriched meals is high and at similar level on an oil freebasis. Dry separation by screening to separate the extracted meal intothe protein and fiber enriched meals did not alter the concentration oftotal aliphatic glucosinolates significantly. Wet separation processingreduced the total aliphatic glucosinolates dramatically from 17.31μmoles/g in the protein enriched meal to 0.11 μmole/g in canola proteinconcentrate, 0.23 μmole/g in hydrolyzed protein concentrate and0.17-0.41 μmole/g in protein isolate.

Accordingly, based on the above described properties of the canolaprotein concentrates and isolates, the concentrates and isolates have:

-   -   (a) Excellent nutritional value and the only vegetable protein        product having high lysine and methionine. For example, protein        isolates of the present disclosure will typically have greater        than 4.5% lysine by weight and 2.0% methionine by weight of the        isolate as a whole. Further, protein concentrates of the present        disclosure will typically have greater than 5.4% lysine by        weight and 1.9% methionine by weight of the concentrate as a        whole;    -   (b) Attractive labeling as GMO free and no food allergies;    -   (c) Zero or very low fat. Typically, the protein isolates of the        present disclosure will have less than 0.2% fat by weight of the        protein isolate as a whole, while the protein concentrates will        typically have less than 0.5% fat by weight of the protein        concentrate as a whole;    -   (d) Vegetable protein origin and green products;    -   (e) Gluten free;    -   (f) Low salt and low sugar contents. Typically, the protein        isolates of the present disclosure will have less than 0.5%        sugar by weight and less than 0.5% salt by weight of the protein        isolate as a whole. Further, the protein concentrates of the        present disclosure will have less than 0.5% sugar by weight and        about 0% salt by weight of the protein isolate as a whole.

Example 6 Canola Protein Concentrate Having about 70% Protein Content(i) Milling and Screening of Defatted Juncea Meal

Approximately 458.5 kg of defatted canola meal (prepared as in Example4) was milled using a disc mill equipped with #8114 stationary androtating plates (The Bauer Bros. Co., Springfield, Ohio, U.S.A.) at0.02″ gap, 2340 rpm rotational speed and 100 kg/hr throughput. Only onepass through the disc mill was conducted. Approximately 448 kg of milledcanola meal was produced. Approximately 10.5 kg of material was lost inthe milling operation with a recovery yield of 97.71%.

Approximately 300 kg of the milled canola meal was screened through a 45US mesh screen using the Rotex Vibratory Screen at a feed rate of 100kg/hr. Only one pass through the screen was conducted. Approximately 131kg of protein enriched meal (fine fraction) and 165 kg of fiber enrichedmeal (coarse fraction) were produced, respectively. Approximately 4 kgof material was lost in the screening operation with a recovery yield of98.67%. After screening, 44.26% of the total material was proteinenriched meal and 55.74% was fiber enriched meal, respectively. Aschematic representation illustrating milling and screening of defattedJuncea meal is shown in FIG. 23.

(ii) Wet Separation to Remove Fiber

Approximately 100 kg of the protein enriched meal was mixed with 800 kgof tap water at a ratio of 1 to 8 (by weight) under homogeneousagitation. The protein slurry was adjusted to about pH 7 by slowaddition of 2.8 kg of 11.06% NaOH solution under homogeneous agitation.This was followed by centrifugation at room temperature using a BirdDecanter Centrifuge (Bird 6″ Continuous Bowl Centrifuge, Bird MachineCompany of Canada, Saskatoon, Saskatchewan) at 1500 rpm bowl speed and alow pool depth. A schematic flowchart illustrating the wet separationand removal of fiber is shown in FIG. 24.

The protein slurry was pumped through the Bird Decanter at ambienttemperature and a feed rate of 150 kg/hr and it was operated at a bowlspeed of 1,500 rpm and a low pool depth to separate the coarse fibersolids from the soluble and insoluble protein fractions. Approximately203.9 kg of wet fiber solids containing 16.4% solids and 698.9 kg ofprotein slurry containing soluble and insoluble proteins at 8.7% solidswere produced, respectively. 698.9 kg of protein slurry containingsoluble and insoluble proteins would be used to produce proteinconcentrate.

Approximately 203.9 kg of wet fiber solids was mixed with 502 kg ofwater in a tank for 0.5 hour, which was followed by centrifugation toseparate the soluble liquid extract from the insoluble fiber solids atroom temperature using the Bird Decanter at a bowl speed of 4,000 rpmand a feed rate of 350 kg/hr. Approximately 126.3 kg of insoluble fibersolids and 579.5 kg of soluble liquid extract were produced. Theinsoluble fiber solids are used to produce hydrolyzed proteinconcentrate.

(iii) Preparation of Protein Concentrate

Approximately 698.9 kg of protein slurry containing soluble andinsoluble proteins after the fiber removal in the using the BirdDecanter was mixed with 650 liters of SDAG 13 denatured ethanol(containing 99% ethanol and 1% ethyl acetate) for 1 hour at roomtemperature. This was followed by centrifugation using a Wesffalia®Decanter to obtain 889.1 kg of a first sugar extract containing 1.89%solids and 307.9 kg of a wet protein solids fraction containing 14.07%solids. The wet protein solids fraction (307.9 kg) was mixed with 332 kgof SDAG 13 denatured ethanol for 1 hour at room temperature. This wasagain followed by centrifugation using the Westfalia® Decanter to obtain429.7 kg of a second sugar extract and 210.2 kg of a second wet proteinsolid fraction. Finally, the wet protein solids (210.2 kg) were mixedwith 336 kg of SDAG 13 denatured ethanol for 1 hour at room temperature,which was followed by centrifugation using the Westfalia® Decanter toobtain 351.8 kg of a third sugar extract and 194.4 kg of a third wetprotein solid fraction. The wet protein solids fractions were dried at50±3° C. under vacuum using a Littleford® Dryer until the moisturecontent was about 7.83%. The protein concentrate contained 68.2% proteinon a dry weight basis. A schematic flowchart illustrating thepreparation of a protein concentrate is shown in FIG. 25.

(iv) Preparation of Hydrolyzed Protein Concentrate

Approximately 126.3 kg of insoluble fiber solids were mixed with 100 kgof water in a tank. This was followed by pH adjustment to 8.3±0.1 using0.9 kg of 11.06% NaOH solution. Approximately 0.5 kg of a first protease(Alcalase® 2.4 L FG) was added to the slurry. The slurry was then heatedto 60±2° C. and held at this temperature for 4 hours. The slurry wascooled down to 50±2° C. and pH adjusted to 6.5. Approximately 0.5 kg ofa second protease (Flavouzyme) was added to the slurry, which wasfollowed by holding at 50±2° C. for 4 hours. The slurry was centrifugedusing the Westfalia® Decanter at 3300×g to separate the hydrolyzedprotein extract from the insoluble fiber fraction. The insoluble fiberwas washed further with 120 kg of filtered tap water, which was againfollowed by centrifugation at 3300×g to separate the wash proteinextract from the washed fiber solids using the Westfalia® Decanter. Thehydrolyzed protein extract and the wash hydrolyzed protein extract werecombined. The combined hydrolyzed protein extract was fed to aMillipore® Ultrafiltration Unit (Model A60, Millipore® Corporation,Bedford, Mass., USA) at ambient temperature. The Ultrafiltration Unit(UF) was fitted with three hollow fiber cartridges with a molecularweight cutoff of 10,000 daltons, with each cartridge containing 5 m² ofmembrane surface area. The hydrolyzed protein extract was pumped throughthe hollow fiber cartridges at a rate of 800-1000 kg/hr. The retentatewas recycled back to the feed tank and the permeate was collected inanother tank. The UF unit was operated at an inlet pressure of 25 psimaximum and a retentate back pressure of 15 psi maximum. The flux rateor permeate rate was about 190-300 kg/hr throughout the ultrafiltrationprocess. The ultrafiltration process continued until about 40 kg ofretentate remained in the feed tank. Approximately 260 kg of water wasadded continuously into the feed tank and ultrafiltration was conductedat ambient temperature using the same UF unit fitted with the same threehollow fiber cartridges. The original volume of retentate in the feedtank was held constant by adding water to make up for the removedpermeate. The retentate was recycled back to the feed tank. Theultrafiltration process continued until all 260 kg of water was added tothe retentate. A schematic flowchart illustrating the preparation of ahydrolyzed protein concentrate is shown in FIG. 26.

Approximately 540 kg of permeate and 47.7 kg of retentate were obtainedfrom the ultrafiltration process. The permeate was spray dried toproduce hydrolyzed protein concentrate using a Komline Sanderson® spraydryer (Komline Sanderson® Ltd., Brampton, Ontario, Canada). The spraydrying operation was conducted at an inlet air temperature of 185±5° C.and an outlet air temperature of 85±5° C. Approximately 3.36 kg of spraydried hydrolyzed protein concentrate containing 82% protein (dwb) wasproduced.

Discussion

The results of the proximate analysis for defatted canola meal, proteinenriched meal, fiber enriched meal, protein concentrate and hydrolyzedprotein concentrate are shown in Table 36. As shown in Table 36, dryseparation by milling using a disc mill and screening using a vibratoryscreen of 45 US mesh increased the protein content from 48% in thedefatted meal to 51.5% in the protein enriched meal. The fiber contentwas reduced from 7.75% in the extracted meal to 5.48% in the proteinenriched meal by dry separation. Wet separation to remove fiber usingthe Bird Decanter and to remove sugar compounds by the ethanolextraction process further increased the protein content from 51.5% inthe protein enriched meal to 68.2% in the protein concentrate.

The enhancement in the protein content by ethanol washing is shown inTable 37. The protein content in the ethanol washed protein solids wasincreased to 61.4%, 66.3% and 67.8% in the ethanol precipitation, firstand second ethanol washings. The large increase in the protein contentwas achieved in the 1^(st) ethanol washing of the ethanol precipitatedprotein solids, from 61.4% protein to 66.3% protein.

In order to produce a protein concentrate containing about 70% protein(dwb), it is necessary to separate and remove fiber from the solubleprotein extract and the insoluble protein particles taking advantage ofthe difference in density and particle size between the fiber andinsoluble protein particles. The protein enriched meal was mixed withwater at a ratio of 1 to 8 by weight and pH was adjusted to 7.0. After 1hour of holding time under agitation at room temperature, the proteinslurry was centrifuged at a low bowl speed of 1,500 RPM (˜750 g force)using the Bird Decanter. Larger fiber particles with higher density wereseparated from smaller insoluble protein particles with lower density aswell as soluble protein solution. In an embodiment, the soluble proteinextract would be re-cycled and re-used to increase the soluble solidcontent in order increase the density and viscosity of the liquidmedium, which would help to reduce the volume of water usage.

Hydrolyzed protein concentrate containing 82% protein (dwb) wasobtained. The hydrolyzed protein concentrate was 100% water soluble andits solution was crystal clear since it was purified by a membranefiltration process. A shown in Table 38, the protein recovery yieldthrough protein hydrolysis and membrane purification was about 85.15%before spray drying, which was calculated based on the hydrolyzedproteins including amino acids and peptides in the permeate of theultrafiltration divided by the total proteins in the starting materialof the insoluble fiber solids before the hydrolysis process (6.88 kg ofprotein weight in the permeate divided by 8.08 kg of protein weight inthe insoluble fiber solids gave 85.15% protein recovery yield). The lossof proteins through membrane filtration is about 3.22% (0.26 kg ofprotein weight in the retentate divided by 8.08 kg of protein weight inthe permeate gives 3.22% protein loss in the UF process).

The hydrolyzed protein concentrate produced in accordance with theprocesses of the present disclosure contained 82% protein (dwb). It wasdetermined that the protein dispersibility index of the hydrolyzedprotein concentrate was 99.8% and its solution was clear and transparentsince it was purified by a membrane filtration process. The absorbanceand transmittance of 1%, 3% and 5% hydrolyzed protein solutions usingdistilled water as the control is shown in Table 39. The absorbance andtransmittance of 1% soy and pea protein isolate solutions were alsodetermined for comparison. The absorbance and transmittance of thesamples were determined at 720 nm wavelength using a Shimadzu®UV-Visible Spectrophotometer (UV-VIS 265, Mandel Scientific® CompanyLtd., Guelph, Ontario, Canada).

In spectroscopy, the absorbance A and transmittance I_(out)/I_(in) at720 nm wavelength are defined as:

A _(720 nm)=−log₁₀(I _(out) /I _(in))  (I)

-   -   I_(out) is the intensity of light at 720 nm wavelength that has        passed through a sample (transmitted light intensity).    -   I_(in) is the intensity of the light before it enters the        sample.

As shown in Table 39, 97%, 89% and 87% light intensity passed through1%, 3% and 5% hydrolyzed canola protein concentrate solutions at 720 nmwavelength. These hydrolyzed protein solutions were clear andtransparent by visual inspection. In comparison, less than 0.016% lightintensity had passed through 1% soy and pea protein isolate solutions.The soy and pea protein isolate solutions were not clear andtransparent. The incident light was likely scattered by the dispersedparticles in the soy and pea protein isolate solutions.

Example 7 Canola Protein Concentrate Having about 65-75% Protein Content

(i) Preparation of Defatted Meal from Regular Canola Seed (B. napus)

Approximately 10 kg of regular canola seed (B. napus) was adjusted to 9%moisture by adding water to the canola seed in a plastic pail withmanual agitation for a few minutes. The canola seed in the pail was thencovered and tempered overnight in the laboratory. The moisture adjustedregular canola seed was then heated in a microwave oven for 2 minutes(heat to 85-95° C.). The canola seed was then covered with an aluminumfoil and heated at 95° C. in a forced air oven for 30 minutes. After theheat treatment, the regular canola seed was flaked using a lab flakingmill. The flaked and heat treated seed was pressed using a GustaLaboratory Screw Press. Approximately 3.26 kg of press oil and 6.32 kgof press cake were obtained from the pressing operation.

Approximately 6.32 kg of regular canola press cake was extracted with 16liters of methyl pentane for 5 hours using a Soxhlet extraction systemto obtain an extracted oil and a defatted canola meal. The extracted oilwas recovered by evaporation and desolventization to remove the solventfrom the miscella under vacuum at 60° C.

The methyl pentane defatted regular canola meal was desolventized in alaboratory fume hood for three days at room temperature. Approximately5.02 kg of defatted regular canola meal was obtained afterdesolventization and drying.

(ii) Preparation of Defatted Meal from Juncea Seed (B. juncea)

Approximately 499 kg of cleaned Juncea seed containing 8.12% moisturewas flaked to produce flaked seed with an average thickness of 0.3±0.1mm using a flaking mill (Model S28, Lauhoff Corporation, Detroit,U.S.A.). The flaked canola seed was heat treated using a two traycooker. The temperature for the top tray was 52-59° C., while thetemperature for the bottom tray was 68-90° C. The resident time for thetop and bottom trays was 20 minutes, respectively. After heat treatment,the flaked seed was fed into the press and pressed to produce 278.9 kgof press cake and 138.1 kg of press oil.

Approximately 10 kg of canola (Juncea) press cake was extracted with 32liters of methyl pentane for 5 hours using a Soxhlet extraction systemto obtain extracted oil and defatted canola meal. The extracted oil wasrecovered by evaporation and desolventization to remove the solvent fromthe miscella under vacuum at 60° C. The methyl pentane defatted canolameal was desolventized in a laboratory fume hood for three days at roomtemperature. Approximately 8.23 kg of defatted canola (Juncea) meal wasobtained.

(iii) Lab Milling and Screening of Defatted Regular (napus) and JunceaMeals

Approximately 4.01 kg of defatted regular canola meal was milled for 1minute using a lab Warring Blender, which was followed by manualscreening using a 45 US mesh Rotex screen to generate a protein enrichedfraction (fine fraction) and a fiber enriched fraction (coarsefraction). The coarse fraction was re-milled in the lab Warring Blenderfor 1 minute. This was followed by manual screening using the 45 US meshRotex screen to generate a second protein enriched fraction and a coarsefraction. Finally, the coarse fraction was milled in the Warring Blenderfor 1 minute and the milled material was manually screened using the 45US mesh Rotex screen to generate a third protein enriched fraction andthe final fiber enriched meal. Approximately 1.76 kg of combined proteinenriched fractions and 2.24 kg of fiber enriched meal were produced,respectively. Therefore, 43.89% of the total material was the proteinenriched meal and 56.11% was the fiber enriched meal.

Approximately 3.52 kg of defatted Juncea meal was milled for 1 minuteusing a lab Warring Blender, which was followed by manual screeningusing a 45 US mesh Rotex screen to generate a protein enriched fraction(fine fraction) and a fiber enriched fraction (coarse fraction). Thecoarse fraction was re-milled in the lab Warring Blender for 1 minute.This was followed by manual screening using the 45 US mesh Rotex screento generate a second protein enriched fraction and a coarse fraction.Finally, the coarse fraction was milled in the Warring Blender for 1minute and the milled material was manually screened using the 45 USmesh Rotex screen to generate a third protein enriched fraction and thefinal fiber enriched meal. Approximately, 1.53 kg of combined proteinenriched fractions and 1.84 kg of fiber enriched meal were produced,respectively. Therefore, 43.71% of the total material was the proteinenriched meal and 56.29% was the fiber enriched meal. The mass balancedata for preparation of defatted meals, protein and fiber enriched mealsare given in Table 40.

(iv) Wet Separation to Remove Fiber

Approximately 0.75 kg regular (napus) protein enriched meal was mixedwith 6 kg of water at a ratio of 1 to 8 by weight at ambient temperaturefor 1 hour under homogeneous agitation. The protein slurry wascentrifuged at 4,000 rpm for 10 minutes using a lab centrifuge. Threelayers of top liquid layer, the middle insoluble protein layer and thebottom insoluble fiber layer were obtained in the centrifuge bottles.The larger fiber particles with higher density settled faster than thesmaller insoluble protein particles with lower density. Therefore, thelarger fiber particles settled to the bottom of the bottles at first.The smaller insoluble protein particles with lower density settled onthe top of the fiber layer. The liquid extract containing solubleproteins was at the top layer. The bottom fiber layer (0.347 kg) wasseparated manually from the middle insoluble protein layer (1.360 kg)and the top liquid extract layer (5.053 kg). After the fiber removal,the middle insoluble protein layer and the top liquid extract layer werecombined and the combined slurry was mixed with 100% SDAG 13 ethanol ata ratio of 1 to 1 by volume for 10 minutes to precipitate proteins. Theprecipitation slurry was centrifuged at 4,000 rpm for 10 minutes toseparate the soluble sugar extract from the insoluble protein solidsusing the lab centrifuge. The recovered protein solids were mixed with4.5 kg of 80% ethanol (v/v) at ambient temperature for 1 hour, which wasfollowed by centrifugation at 4,000 rpm for 10 minutes to separate theinsoluble protein solids from the washing sugar extract. Finally, theinsoluble protein solids were mixed with 4.5 kg of 80% ethanol (v/v) atambient temperature for 1 hour. The slurry was once again centrifuged at4,000 rpm to separate the washed protein solids from the soluble sugarextract. The washed protein solids were desolventized in a laboratoryfume hood for 3 days before drying to 5.26% moisture at 50° C. using aforced air oven. The dried protein concentrate was milled into powderform using a lab pin mill.

Approximately 1 kg of Juncea protein enriched meal was mixed with 8 kgof water at a ratio of 1 to 8 by weight at ambient temperature for 1hour under homogeneous agitation. The protein slurry was centrifuged at4,000 rpm for 10 minutes using the lab centrifuge. Three layers of topliquid layer, the middle insoluble protein layer and the bottominsoluble fiber layer were obtained in the centrifuge bottles. Thelarger fiber particles with higher density settled faster than thesmaller insoluble protein particles with lower density. Therefore, thelarger fiber particles settled to the bottom of the bottles at first.The smaller insoluble protein particles with lower density settled onthe top of the fiber layer. The liquid extract containing solubleproteins was at the top layer. The bottom fiber layer (0.430 kg) wasseparated manually from the middle insoluble protein layer (2.282 kg)and the top liquid extract layer (6.288 kg). After the fiber removal,the middle insoluble protein layer and the top liquid extract layer werecombined and the combined slurry was mixed with 100% SDAG 13 ethanol ata ratio of 1 to 1 by volume for 10 minutes to precipitate proteins. Theprecipitation slurry was centrifuged at 4,000 rpm for 10 minutes toseparate the soluble sugar extract from the insoluble protein solidsusing the lab centrifuge. The recovered protein solids were mixed with 6kg of 80% ethanol (v/v) at ambient temperature for 1 hour, which wasfollowed by centrifugation at 4,000 rpm for 10 minutes to separate theinsoluble protein solids from the washing sugar extract. Finally, theinsoluble protein solids were mixed with 6 kg of 80% ethanol (v/v) atambient temperature for 1 hour. The slurry was once again centrifuged at4,000 rpm to separate the washed protein solids from the soluble sugarextract. The washed protein solids were desolventized in a laboratoryfume hood for 3 days before drying to 3.9% moisture at 50° C. using aforced air oven. The dried protein concentrate was milled into powderform using a lab pin mill. The mass balance data for the wet separationprocess to remove fiber and prepare protein concentrate are shown inTable 41.

Discussion

As shown in Table 42, the protein content was increased from 46.8% (dwb)in the defatted regular canola meal to 51.5% (dwb) in the regularprotein enriched meal by the milling and screening operation. The crudefiber content was reduced from 9.90% (dwb) in the defatted regularcanola meal to 7.09% (dwb) in the regular protein enriched meal. Theprotein content was increased from 48.7% (dwb) in the defatted Junceameal to 52.8% (dwb) in the Juncea protein enriched meal by the millingand screening operation. The crude fiber content was reduced from 7.44%(dwb) in the defatted Juncea meal to 5.36% (dwb) in the Juncea proteinenriched meal. A simple step of dry milling and screening was able toreduce fiber and increase protein content.

As shown in Table 43, the wet separation process to remove fiber bycentrifugation based on the particle size and density difference ofinsoluble fiber and protein particles as well as to remove sugarcompounds by the ethanol extraction process increased the proteincontent from 51.5% in the regular protein enriched meal to 66.9% in theregular protein concentrate. The protein content was increased from52.8% in the Juncea protein enriched meal to 71.2% in the Juncea proteinconcentrate by the wet fiber separation and ethanol washing process.

The amino acid profile of defatted canola meals and protein concentratesis shown in Table 44. Canola protein concentrates generated from themethyl pentane defatted regular and Juncea canola meals contains higherlysine and sulphur containing amino acids methionine and cystine thanthe canola protein concentrate generated from the defatted Juncea mealusing a solvent mixture of butane and R134a (see Example 5). From theamino acid profile, canola protein concentrates are of high nutritionalquality and capable of providing adequate amounts of all essential aminoacids. From the essential amino acid profiles as shown in Table 44,canola protein concentrates are rich in the muscle building essentialamino acids such as valine, methionine, leucine and isoleucine. Theyalso contain a high content of the essential amino acid threonine, whichis important for brain activity. Both regular and Juncea canola proteinconcentrates generated from methyl pentane defatted meals containsimilar content of essential amino acids.

In an embodiment of the disclosure, the canola protein concentratesproduced in accordance with the present disclosure, contain about 2% toabout 8% crude fiber and 65-75% protein on a dry weight basis. In afurther embodiment, the protein concentrates have a minimum 25% solubleprotein in a borate-phosphate buffer solution. In a further embodimentof the disclosure, the hydrolyzed canola protein concentrates containstypically less than about 5%, optionally 2% and suitably about 0% crudefiber, and greater than about 75% protein on a dry weight basis. Inanother embodiment, the hydrolyzed protein concentrate is at least about95%, optionally about 98%, optionally about 99% and suitably about 100%water soluble. In an embodiment, the hydrolyzed protein concentrate hasa 100% water solubility as defined by 100% PDI value (proteindispersibility index). In another embodiment of the disclosure, thecanola protein isolates produced in accordance with the presentdisclosure typically contain about 0% crude fiber and greater than about90% protein. In another embodiment, the protein isolates have a minimumof about 85% soluble protein in a borate-phosphate buffer solution. Inanother embodiment, the protein isolates have a typical molecular weighprofile of 64.7% at 70 kDa, 26.2% at 12 kDa and 9.1% at <kDa.

The results of protein solubility test on defatted canola meals andprotein concentrates are shown in Table 45. The test results show thatthe defatted regular and Juncea meals have similar protein solubility of30.36-31.48% while regular and Juncea proteins concentrates have proteinsolubility of 32.27-36.76%. They all have much higher protein solubilitythan commercially available samples of soy and pea protein isolates.

The results of antinutritional factors in defatted canola meals, canolaprotein concentrates, canola protein isolate and commercial samples ofsoy and pea protein isolates are shown in Table 46. The wet separationand ethanol washing process for preparation of canola proteinconcentrates from defatted meals had significantly reduced the sinapinecontent. Canola protein concentrates contain similar sinapine content ascommercial samples of soy and pea protein isolates. Canola proteinconcentrates contain higher phytate content than soy and pea proteinisolates. Canola protein isolate contains lower phytate content than soyand pea protein isolates.

Example 8 Canola Protein Concentrate Having about 73% Protein Content(i) Preparation of Defatted Meal

A press cake was produced from Juncea seed (B. juncea) using theprocessing conditions similar to those listed in Example 5. DefattedJuncea meal was produced from the press cake through solvent extractionat 50° C. for 1.5 hours using a solvent mixture of butane and R134a. Thedefatted meal was milled using a disc mill equipped with #8114stationary and rotating plates (The Bauer Bros. Co., Springfield, Ohio,U.S.A.) at 0.02″ gap, 2340 rpm rotational speed and 100 kg/hrthroughput. Only one pass through the disc mill was conducted.

(ii) Wet Separation to Remove Fiber

(a) A schematic flowchart for wet fiber separation is shown in FIG. 27.

Approximately 10 kg of defatted meal was mixed with 80 kg of tap waterat a ratio of 1 to 8 (by weight) under homogeneous agitation for 1 hour.The pH of protein slurry was at 7.6 and no further pH adjustment wasrequired. The canola meal slurry was centrifuged at ambient temperatureusing a Bird Decanter Centrifuge (Bird 6″ Continuous Bowl Centrifuge,Bird Machine Company of Canada, Saskatoon, Saskatchewan) at 1500 rpmbowl speed and a low pool depth. The canola meal slurry was pumpedthrough the Bird Decanter at ambient temperature and a feed rate of 150kg/hr and it was operated at a bowl speed of 1,500 rpm and a low pooldepth to separate the coarse fiber solids from the soluble and insolubleprotein fractions. Approximately 30.58 kg of wet fiber solids #1Acontaining 16.65% solids and 46.5 kg of protein slurry #1A containingsoluble and insoluble proteins at 6.31% solids were produced,respectively.

The wet fiber solids #1A was mixed with 61.16 kg of water in a tank for15 minutes, which was followed by centrifugation to separate the washedfiber solids #1B from the insoluble protein solids and soluble proteinextract #1B at room temperature using the Bird Decanter at a bowl speedof 1,500 rpm and a feed rate of 150 kg/hr. Approximately 23.77 kg ofwashed fiber solids #1 B containing 17.28% solids and 58 kg of insolubleand soluble protein slurry #1 B containing 1.9% solids were produced.

The insoluble protein solids and soluble protein extract #1A and #1Bwere combined, which was followed by centrifugation using the BirdDecanter at 5,000 rpm to separate the insoluble protein solids #1C fromthe soluble and insoluble protein slurry #1C. Approximately 1.68 kg ofinsoluble protein solids #1C containing 10.57% solids and 96.5 kg ofsoluble and insoluble protein slurry #1C containing 4.34% solids wereproduced.

(b) Recycling of Protein Slurry Containing Soluble and Insoluble ProteinFractions

A schematic flowchart for wet fiber separation and the 1^(st) recycle isshown in FIG. 28. Approximately 10 kg of defatted meal was mixed with96.5 kg of soluble and insoluble protein slurry #1C generated from theprevious wet fiber separation process under homogeneous agitation for 1hour. The pH of protein slurry was at 7.6 and no further pH adjustmentwas required. The canola meal slurry was centrifuged at ambienttemperature using a Bird Decanter Centrifuge (Bird 6″ Continuous BowlCentrifuge, Bird Machine Company of Canada,

Saskatoon, Saskatchewan) at 1,500 rpm bowl speed and a low pool depth.The canola meal slurry was pumped through the Bird Decanter at ambienttemperature and a feed rate of 150 kg/hr to separate the coarse fibersolids from the soluble and insoluble protein fractions. Approximately32.1 kg of wet fiber solids #2A containing 19.02% solids and 64 kg ofprotein slurry #2A containing soluble and insoluble proteins at 8.81%solids were produced, respectively.

The wet fiber solids #2A was mixed with 46.8 kg of water in a tank for15 minutes, which was followed by centrifugation to separate the washedfiber solids #2B from the insoluble protein solids and soluble proteinextract #2B at ambient temperature using the Bird Decanter at a bowlspeed of 1,500 rpm and a feed rate of 150 kg/hr. Approximately 20.25 kgof washed fiber solids #2B containing 18.34% solids and 47 kg ofinsoluble and soluble protein slurry #2B containing 6.12% solids wereproduced.

The insoluble protein solids and soluble protein extract #2A and #2Bwere combined, which was followed by centrifugation using the BirdDecanter at 5,000 rpm to separate the insoluble protein solids #2C fromthe soluble and insoluble protein slurry #2C. Approximately 3.0 kg ofinsoluble protein solids #2C containing 8.49% solids and 112 kg ofsoluble and insoluble protein slurry #2C containing 6.83% solids wereproduced.

(c) Second Recycling

A schematic flowchart for wet fiber separation and the 2^(nd) recycle isshown in FIG. 29. Approximately 10 kg of defatted meal was mixed with112 kg of soluble and insoluble protein slurry #2C generated from theprevious wet fiber separation process under homogeneous agitation for 1hour. The pH of protein slurry was at 7.6 and no further pH adjustmentwas required. The canola meal slurry was centrifuged at ambienttemperature using a Bird Decanter Centrifuge (Bird 6″ Continuous BowlCentrifuge, Bird Machine Company of Canada, Saskatoon, Saskatchewan) at1,500 rpm bowl speed and a low pool depth. The canola meal slurry waspumped through the Bird Decanter at ambient temperature and a feed rateof 150 kg/hr to separate the coarse fiber solids from the soluble andinsoluble protein fractions. Approximately 49.4 kg of wet fiber solids#3A containing 17.54% solids and 67.0 kg of protein slurry #3Acontaining soluble and insoluble proteins at 9.87% solids were produced,respectively.

The wet fiber solids #3A was mixed with 74 kg of water in a tank for 15minutes, which was followed by centrifugation to separate the washedfiber solids #3B from the insoluble protein solids and soluble proteinextract #3B at ambient temperature using the Bird Decanter at a bowlspeed of 1,500 rpm and a feed rate of 150 kg/hr. Approximately 22.2 kgof washed fiber solids #3B containing 17.92% solids and 90.5 kg ofinsoluble and soluble protein slurry #3B containing 5.32% solids wereproduced.

The insoluble protein solids and soluble protein extract #3A and #3Bwere combined, which was followed by centrifugation using the BirdDecanter at 5,000 rpm to separate the insoluble protein solids #3C fromthe soluble and insoluble protein slurry #3C. Approximately 4.74 kg ofinsoluble protein solids #3C containing 8.41% solids and 112.5 kg ofsoluble and insoluble protein slurry #3C containing 5.89% solids wereproduced.

(d) Third Recycling

A schematic flowchart for wet fiber separation and the 3^(rd) recycle isshown in FIG. 30. Approximately 10 kg of defatted meal was mixed with112.5 kg of soluble and insoluble protein slurry #3C generated from theprevious wet fiber separation process under homogeneous agitation for 1hour. The pH of protein slurry was at 7.6 and no further pH adjustmentwas required. The canola meal slurry was centrifuged at ambienttemperature using a Bird Decanter Centrifuge (Bird 6″ Continuous BowlCentrifuge, Bird Machine Company of Canada, Saskatoon, Saskatchewan) at1500 rpm bowl speed and a low pool depth. The canola meal slurry waspumped through the Bird Decanter at ambient temperature and a feed rateof 150 kg/hr to separate the coarse fiber solids from the soluble andinsoluble protein fractions. Approximately 29.1 kg of wet fiber solids#4A containing 20.46% solids and 77.0 kg of protein slurry #4Acontaining soluble and insoluble proteins at 9.63% solids were produced,respectively.

The wet fiber solids #4A was mixed with 33.3 kg of water in a tank for15 minutes, which was followed by centrifugation to separate the washedfiber solids #4B from the insoluble protein solids and soluble proteinextract #4B at ambient temperature using the Bird Decanter at a bowlspeed of 1,500 rpm and a feed rate of 150 kg/hr. Approximately 19.88 kgof washed fiber solids #4B containing 18.23% solids and 42.5 kg ofinsoluble and soluble protein slurry #4B containing 6.56% solids wereproduced.

The insoluble protein solids and soluble protein extract #4A and #4Bwere combined, which was followed by centrifugation using the BirdDecanter at 5,000 rpm to separate the insoluble protein solids #4C fromthe soluble and insoluble protein slurry #4C. Approximately 2.2 kg ofinsoluble protein solids #4C containing 15.27% solids and 102.5 kg ofsoluble and insoluble protein slurry #4C containing 7.97% solids wereproduced.

(e) Fourth Recycling

A schematic flowchart for wet fiber separation and the 4^(th) recycle isshown in FIG. 31. Approximately 10 kg of defatted meal was mixed with112.5 kg of soluble and insoluble protein slurry #4C generated from theprevious wet fiber separation process under homogeneous agitation for 1hour. The pH of protein slurry was at 7.6 and no further pH adjustmentwas required. The canola meal slurry was centrifuged at ambienttemperature using a Bird Decanter Centrifuge (Bird 6″ Continuous BowlCentrifuge, Bird Machine Company of Canada, Saskatoon, Saskatchewan) at1,500 rpm bowl speed and a low pool depth. The canola meal slurry waspumped through the Bird Decanter at ambient temperature and a feed rateof 150 kg/hr to separate the coarse fiber solids from the soluble andinsoluble protein fractions. Approximately 32.0 kg of wet fiber solids#5A containing 20.32% solids and 86.5 kg of protein slurry #5Acontaining soluble and insoluble proteins at 12.46% solids wereproduced, respectively.

The wet fiber solids #5A was mixed with 48 kg of water in a tank for 15minutes, which was followed by centrifugation to separate the washedfiber solids #5B from the insoluble protein solids and soluble proteinextract #5B at ambient temperature using the Bird Decanter at a bowlspeed of 1,500 rpm and a feed rate of 150 kg/hr. Approximately 18.5 kgof washed fiber solids #5B containing 20.71% solids and 56.5 kg ofinsoluble and soluble protein slurry #5B containing 3.94% solids wereproduced.

The insoluble protein solids and soluble protein extract #5A and #5Bwere combined, which was followed by centrifugation using the BirdDecanter at 5,000 rpm to separate the insoluble protein solids #5C fromthe soluble and insoluble protein slurry #5C. Approximately 3.2 kg ofinsoluble protein solids #5C containing 11.39% solids and 132 kg ofsoluble and insoluble protein slurry #5C containing 9.03% solids wereproduced.

(f) Fifth Recycling

A schematic flowchart for wet fiber separation and the 5^(th) recycle isshown in FIG. 32. Approximately 10 kg of defatted meal was mixed with132 kg of soluble and insoluble protein slurry #5C generated from theprevious wet fiber separation process under homogeneous agitation for 1hour. The pH of protein slurry was at 7.6 and no further pH adjustmentwas required. The canola meal slurry was centrifuged at ambienttemperature using a Bird Decanter Centrifuge (Bird 6″ Continuous BowlCentrifuge, Bird Machine Company of Canada, Saskatoon, Saskatchewan) at1,500 rpm bowl speed and a low pool depth. The canola meal slurry waspumped through the Bird Decanter at ambient temperature and a feed rateof 150 kg/hr to separate the coarse fiber solids from the soluble andinsoluble protein fractions. Approximately 39.5 kg of wet fiber solids#6A containing 20.04% solids and 94.5 kg of protein slurry #6Acontaining soluble and insoluble proteins at 12.04% solids wereproduced, respectively.

The wet fiber solids #6A was mixed with 32 kg of water in a tank for 15minutes, which was followed by centrifugation to separate the washedfiber solids #6B from the insoluble protein solids and soluble proteinextract #6B at ambient temperature using the Bird Decanter at a bowlspeed of 1,500 rpm and a feed rate of 150 kg/hr. Approximately 23.3 kgof washed fiber solids #6B containing 17.68% solids and 42.5 kg ofinsoluble and soluble protein slurry #6B containing 5.60% solids wereproduced.

(iii) Preparation of Canola Protein Concentrate from Recycled ProteinSlurry

A schematic flowchart for preparation of protein concentrate from thedefatted meal slurry after the fiber removal is shown in FIG. 33. 94.5kg of protein slurry containing soluble and insoluble proteins after thefiber removal and 14.82 kg of insoluble protein solids #1C-#5C weremixed with 77.22 kg of SDAG 13 denatured ethanol (containing 99% ethanoland 1% ethyl acetate) for 1 hour at room temperature. This was followedby centrifugation using a Basket Centrifuge (Tolhurst-26 in.Center-Slung, Ametek, Inc., East Moline, Ill., USA) to obtain 121 kg ofsugar extract #1 and ˜40 kg of wet protein solids #1 containing 29.66%solids. The wet protein solids (˜40 kg) were mixed with 73.87 kg of 85%ethanol (v/v) for 1 hour at ambient temperature. This was again followedby centrifugation using the Basket Centrifuge to obtain 60 kg of sugarextract #2 and ˜40 kg of wet protein solid #2 containing 30.67% solids.Finally, the wet protein solids (˜40 kg) were mixed with 74 kg of 85%ethanol (v/v) for 1 hour at ambient temperature, which was followed bycentrifugation using the Basket Centrifuge to obtain 100.3 kg of sugarextract #3 and 13.6 kg of wet protein solid #3 containing 47.53% solids.The wet protein solids #3 was air desolventized in a lab fume hood for 2days, which was followed by drying at 60° C. in a forced air oven untilthe moisture content is below 7%. The protein concentrate contained73.3% protein on a dry weight basis.

Discussion

As shown in Table 47, canola protein concentrate containing 73.3%protein (dwb) and 3.78% crude fiber (dwb) was produced from defattedcanola meal (B. juncea) the wet fiber separation method based on thedensity and particle size difference between the insoluble fiberparticles and the insoluble protein particles. In an embodiment, dryscreening to prepare a protein enriched meal from defatted meal is notrequired, which increases the protein recovery yield in the proteinconcentrate.

As shown in Table 48, after the wet fiber separation by centrifugation,the protein slurry containing soluble and insoluble proteins is recycledto mix with the defatted meal before the fiber separation. The solidcontent of the protein slurry containing soluble and insoluble proteinswas increased from 6.31% solids to 12.46% solids after 4 recyclingtrials. Higher solid content in the canola slurry did not affect thefiber separation by the wet fiber separation process. The proteincontent of the protein slurry containing insoluble and soluble proteinswas increased while the crude fiber content remained at similar levelwith the increased in the solid content (Table 48). Interestingly,canola protein slurry #6A contained 57.6% protein (dwb) and 1.60% crudefiber (dwb) after the fiber separation and before ethanol precipitation.Canola protein concentrate containing 73.3% protein (dwb) and 3.78%crude fiber was produced. In an embodiment, the fiber separation by thedecanter centrifuge based on the density difference results in a lowcrude fiber content in the protein slurry containing soluble andinsoluble proteins after fiber separation and removal.

As shown in Table 49, the 1^(st) ethanol precipitation increased theprotein content to 69.3% (dwb), the 1^(st) ethanol washing increased theprotein content to 70.6% (dwb) and the 2^(nd) ethanol washing increasedthe protein content to 73.3% (dwb). In an embodiment, a one step ethanolprecipitation is sufficient to produce a protein concentrate containing70% protein (dwb) and a low fiber content comparable to soy proteinconcentrate. In another embodiment, a membrane filtration process isconducted on the protein slurry containing soluble and insolubleproteins at high solid content after fiber separation to concentrate andpurify proteins before spray drying to produce protein concentratecontaining 70% protein (dwb). In an embodiment, an ultrafiltration isutilized since the protein slurry at high solid content already hasreasonable purity in terms of protein content.

In an embodiment, the increase in the solid content of the proteinslurry containing soluble and insoluble proteins serves the purpose ofreducing the processing volume and the amount of ethanol usage. Thiswould reduce the size of the equipment, energy consumption, processingcost and capital investment.

Example 9 Hypothetical Example of Preparation of Canola ProteinConcentrate Containing Greater than 70% Protein

A schematic representation for the preparation of canola proteinconcentrate by membrane filtration is shown in FIG. 34. 100 kg ofdefatted meal is mixed with 800 kg of water at a ratio of 1 to 8 (byweight) under homogeneous agitation. This is followed by centrifugationat room temperature using a Decanter Centrifuge at 1500 rpm bowl speedand a low pool depth to separate the insoluble fiber solids from theprotein slurry containing insoluble and soluble proteins. The proteinslurry containing soluble and insoluble proteins after the fiber removalis centrifuged using a Disc Stack Centrifuge at ambient temperature toseparate the soluble protein extract #1 from the insoluble proteinsolids #1. The insoluble protein solids #1 is mixed with water at aratio of 1 to 2 by weight at ambient temperature for 0.5 hour underhomogeneous agitation, which is followed by centrifugation using theDisc Stack Centrifuge to separate soluble protein extract #2 from thewashed insoluble protein solids.

Soluble protein extracts #1 and #2 are combined and the combined extractis adjusted to pH 7.0 by addition of 11% NaOH solution if the pH isbelow 7, which is followed by concentration of the protein extract inthe feed tank to 10-20% solids using a ultrafiltration membrane with amolecular weight cutoff of 10,000-100,000 daltons. The protein extractis pumped through the membrane unit while the retentate is recycled backto the feed tank and the permeate is collected in another tank.

Water is then added into the feed tank and diafiltration is conductedusing the ultrafiltration membrane with a molecular weight cutoff of10,000-100,000 daltons. The original volume of protein solution in thefeed tank is held constant by adding water to make up for the removedpermeate. The retentate is recycled back to the feed tank. Sufficientamount of water is used in the diafiltration process until the retentatecontains 90% protein or higher on a dry weight basis.

The purified protein extract from ultrafiltration and diafiltration ismixed with the washed insoluble protein solids, which is followed bypasteurization (UV or heat). The pasteurized protein slurry containingsoluble and insoluble proteins is spray dried into protein concentratecontaining 70% protein or higher.

Example 10 Hypothetical Example of Preparation of Canola ProteinConcentrate Containing Greater than 70% Protein

A schematic representation for preparation of a canola proteinconcentrate by membrane filtration is shown in FIG. 35. 100 kg ofdefatted meal is mixed with 800 kg of water at a ratio of 1 to 8 (byweight) under homogeneous agitation. This is followed by centrifugationat ambient temperature using a Decanter Centrifuge at 1500 rpm bowlspeed and a low pool depth to separate the insoluble fiber solids fromthe protein slurry #1 containing insoluble and soluble proteins. Theinsoluble fiber solids are mixed with 200 kg of water for 15 minutes atambient temperature, which is followed by centrifugation using theDecanter Centrifuge at 1500 rpm bowl speed and a low pool depth toseparate the washed fiber solids from the protein slurry #2 containinginsoluble and soluble proteins.

Protein slurries #1 and #2 are combined and the combined slurry isadjusted to pH 7.0 by addition of 11% NaOH solution if the pH is below7, which is followed by concentration of the protein slurry in the feedtank to about 20% solids using a microfiltration membrane of 0.1-0.2micron and an ultrafiltration membrane with a molecular weight cutoff of10,000-100,000 daltons. The protein slurry is pumped through themembrane unit while the retentate is recycled back to the feed tank andthe permeate is collected in another tank.

The purified protein slurry from the ultrafiltration process ispasteurized by UV or heat. The pasteurized protein slurry containingsoluble and insoluble proteins is spray dried into protein concentratecontaining 70% protein.

Prophetic Example 11 Protein Concentrate of about 70-75% Protein FiberHydrolysis and Ethanol Washing

The process for preparation of protein-enriched meal is the same as thatof Example 1. Approximately 1 kg of protein-enriched meal is mixed with6 kg of water in a lab Eberbach Waring Blenderunder for 5 minutes tobreakdown the insoluble protein and fiber particles. The protein slurryis added to a beaker and pH of the slurry is adjusted to 5±0.2 undergood agitation using a magnetic stirrer. Approximately 0.5% cellulase orcellulase complex based on the weight of starting protein enriched mealis added to the protein slurry. The slurry is heated to 55-60° C. andheld at this temperature range for 4 hours. After enzymatic reaction, 8kg of 100% (v/v) ethanol is added to the protein slurry, which isfollowed by mixing for 0.5 hour at 55-60° C. The protein slurry iscentrifuged at 4,000 g force for 15 minutes to separate the proteinsolids from the sugar extract. The sugar extract is concentrated anddried to produce a dried sugar and fraction. The protein solids aredried under vacuum to produce a protein concentrate containing 70-75%protein on a dry weight basis.

Prophetic Example 12 Protein Concentrate of 80% Protein and ProteinIsolate of 90% Protein

Fiber Removal by Screening and Centrifugation 1,000 kg of canola seed at7-10% moisture is conditioned at 80±5° C. for 30±10 minutes in a stackcooker, which is followed by pressing using a DeSmet mini press.Approximately 800 kg of pressed cake and 200 kg of pressed oil areproduced. The pressed cake has a PDI (protein dispersibility index) of30-35. The pressed cake is extracted with hexane at 55-60° C. for 1 hourusing a Crown counter-current extractor at a ratio of hexane to cake of2 to 1 by weight. The extracted meal is desolventized and dried at 50°C. for 5 hours under vacuum using a Littleford® dryer to a solventresidue of less than 500 ppm. Approximately 520 kg of extracted meal isproduced.

The extracted meal is milled using a disc mill at a gap of 0.02″ and themilled meal is screened through a 45 US mesh screen using a RotaryVibratory Screen. Approximately 220 kg of protein enriched meal and 300kg of fiber enriched meal are produced.

Approximately 220 kg of protein enriched meal is mixed with 2,200 kg ofwater under good agitation. The protein slurry is screened through a 40mesh US screen at ambient temperature to remove some fiber. The slurryis adjusted to a pH of 7, which is followed by wet milling through a wetmill (Szego Mill) at ambient temperature. The slurry is centrifugedusing a decanter (Bird Decanter) at ambient temperature to separate therest of fiber from the soluble and insoluble proteins at a bowl speed of1,500 rpm. The slurry of soluble and insoluble proteins is centrifugedagain at ambient temperature to separate the soluble protein solutionfrom the insoluble protein precipitates using a disc stack centrifuge(Wesffalia® Desludger).

The insoluble protein precipitates are washed with water 2 times atambient temperature, and the washed protein precipitates are separatedfrom the washing liquid using a disc stack centrifuge at ambienttemperature. The washed protein precipitates are mixed with 2 parts ofwater and pH of the slurry is adjusted to pH7 at ambient temperature.The slurry of protein precipitates is spray dried using a spray dryer atan inlet temperature of 190° C. and outlet temperature of 85° C. to adried protein concentrate of 80-85% protein on a dry weight basis.

The soluble protein solution recovered from the centrifugationoperations is heated to 45-50° C. before being passed through hollowfiber ultrafiltration cartridge membranes with a molecular weight cutoffof 10,000 daltons. The hollow fiber cartridges are fitted to aMillipore® ultrafiltration unit. The retentate was recycled back to thefeed tank and the permeate is discarded. The ultrafiltration process iscontinued until the amount of protein solution in the feed tank is equalto 25% of its initial weight. After the ultrafiltration is completed,diafiltration is conducted at 45-50° C. using the same ultrafiltrationunit which is fitted with the same hollow fiber cartridges. The originalvolume of protein solution in the feed tank is held constant by addingwater to make up for the removed permeate. The retentate is recycledback to the feed tank. The amount of water received to maintain theoriginal volume of protein solution is 3 times the original volume ofprotein solution. Finally, after all the water is added to the feedtank, the purified protein solution is adjusted to pH7 before it isspray dried into a dried protein isolate containing 90% protein on a dryweight basis using a spray dryer. The spray drying conditions are thesame as those used for the protein concentrate.

Prophetic Example 13 Protein Concentrate of ≧80% Protein and ProteinIsolate of ≧90% Protein Fiber Hydrolysis by Cellulase or CellulaseComplex

The process for preparation of protein enriched meal from canola seed isthe same as that of Prophetic Example 12.

Approximately 220 kg of protein enriched meal is mixed with 2,200 kg ofwater under good agitation. The protein slurry is screened through a 40mesh US screen at ambient temperature to remove some fiber, which isfollowed by wet milling the protein slurry through a wet mill (SzegoMill) at ambient temperature. The protein slurry is centrifuged atambient temperature to separate the soluble protein solution from theinsoluble protein and fiber solids using a disc stack centrifuge(Westfalia® Desludger).

The insoluble solids are mixed with 3 parts of water, which is followedby pH adjustment to 5±0.2. Approximately 0.5% cellulase or cellulasecomplex based on the weight of starting protein enriched meal is addedto the protein slurry. The slurry is heated to 55-60° C. and held atthis temperature range for 4 hours. After enzymatic reaction, theinsoluble protein solids are washed with water following the sameprocess as outlined in Example 4 to produce a protein concentrate of≧80% protein.

The process to produce protein isolate of 90% protein from the solubleprotein solution is the same as that of Example 12.

Example 14 Preparation of Canola Protein Concentrate

A canola protein concentrate was produced from 3,325 kg of lowtemperature defatted canola meal (B. juncea). Seven batches ofprocessing were carried out with 500 kg of defatted meal for six batchesand 325 kg of defatted meal for the last batch. For each batch ofprocessing, defatted canola meal was mixed with tap water at a ratio of1 to 8 by weight. The canola meal slurry was mixed at ambienttemperature for 1 hour before it was pumped to an Andritz® decantercentrifuge (Model D3LVN, Andritz Separation Inc., San Leandro, Calif.,USA) at ambient temperature for the separation of fiber solids fromprotein slurry containing soluble and insoluble proteins. A typical spindown test showed three layers, 50% top supernatant layer, 25% middleinsoluble fine protein solids, and 25% insoluble coarse fiber solids.The decanter centrifuge was operated at the optimum conditions in orderto have a clean separation of the bottom coarse fiber solids (25% of thetotal canola meal slurry) from the protein slurry containing supernatant(50% of the total canola meal slurry) and fine insoluble protein solids(25% of the total canola meal slurry). The operational conditions of thecentrifuge are shown in Table 50, and procedures using low-speedcentrifugation are schematically shown in FIGS. 40-42.

The protein slurry containing supernatant and fine insoluble proteinsolids was immediately mixed with 100% denatured ethanol at a ratio of 1to 1 by volume by pumping the protein slurry into the ethanol in 5600 Lstainless tanks. The proteins precipitated in ethanol. The majority ofprecipitated proteins was recovered by centrifugation using a Westfalia®Decanter (Model CA-365) at 3,200 g (4,000 RPM). The remainingprecipitated proteins in the supernatant were recovered using aWestfalia® Disc Stack Centrifuge (Model SA-14, Germany) at 6,715 g(7,560 rpm). The recovered protein solids were mixed with 85% ethanol(v/v) at ambient temperature for 1 hour. The amount of 85% ethanol (v/v)was equivalent to 6 times of the starting weight of defatted canolameal. The washed protein solids were recovered by centrifugation usingthe Wesffalia® Decanter (Model CA-365) at 3,200 g (4,000 RPM) andambient temperature. The washed protein solids were again mixed with 85%ethanol (v/v) equivalent to 6 times of starting weight of defattedcanola meal. The second washed protein solids were also recovered bycentrifugation using the Westfalia® Decanter (Model CA-365) at 3,200 g(4,000 RPM) and ambient temperature. Finally, the second washed proteinsolids were dried to 3.11-6.66% moisture using a Barr-Rosin ClosedCircuit Ring Dryer. Approximately 760 kg of protein concentrate at69.2-72.7% protein (dwb) was produced from 3,325 kg of defatted canolameal (as seen in Table 51). The produced protein concentrate was a freeflow powder with cream white color. It contained a very lowglucosinolate content of 0.2 μmole/g, a sinapine content of 0.019% and aphytate content of <0.05%.

The recovered yield of canola protein concentrate can be increasedsignificantly by washing of the fiber solids once or twice in order torecover more soluble and insoluble proteins. Ethanol was reclaimed andrecycled from the liquid streams through evaporation and distillationusing a single stage falling film evaporator and a bubble sieve traydistillation system.

As shown in Table 50, the wet fiber separation process by centrifugationat 274-350 g using the Andritz® Decanter (as seen in Table 50) reducedthe crude fiber content to 2.60-3.28% in the protein slurries from 6.98%in the defatted canola meal on a dry weight basis. The crude fibercontent in the fiber solids was increased to 12.14-14.03% (dwb). Ethanolprecipitation process increased the protein content from 52.1-54.2%(dwb) in the protein slurries to 63.8-67.4% (dwb) in the precipitatedproteins. Wash of the precipitated proteins with 85% ethanol (v/v) twicefurther increased the protein content to 69.2-72.7% protein (dwb) in thefinal protein concentrates.

Example 15 Preparation of Canola Protein Isolate Using Phytase

Approximately 62.5 kg of defatted canola meal was mixed with 500 kg ofwater in a tank. Approximately 50 g of phytase (Natuphos® 10,000 LPhytase) at 0.08% dosage based on the starting weight of defatted canolameal was added to the canola meal slurry. The pH of canola meal slurrywas at about 6.0 and temperature between 20° C.-38° C. After holding for1.5 hours under agitation, the protein fraction was separated from thewet solids using an Alfa Laval® decanter centrifuge at maximum g force.

The wet solids were mixed with 331 kg of water in a tank at ambienttemperature for 80 minutes. This was followed by centrifugation usingthe decanter to separate the washing extract from the washed solids.

The protein fractions were combined together and approximately 736 kg ofcombined protein fractions was produced. The combined protein fractionwas clarified using an Alfa Laval® disc stack centrifuge to remove theremaining insoluble solids. Approximately 59 kg of wet solids and 677 kgof clarified protein extract were produced, respectively.

677 kg of clarified protein extract was concentrated at 41-47° C. fromthe initial 2.45% solids to 16% solids at an average flux rate of 58liters per square meter per hour using an Alfa Laval® UF system fittedwith spiral wound membrane (2×GR60PP-3838/80, 6.08 m² total surfacearea) with a molecular weight cut-off of 25,000 Dalton. Purify ofprotein extract was increased from 45% to 85% by ultrafiltration.

Phytase broke phytates through an enzymatic action, which prevented thegel formation of phytates-protein complex on the membrane. This resultedin higher average flux rate and increased the filtration efficiency.

Example 16 Preparation of Canola Protein Isolate Using Phytase DuringFiltration

Approximately 64 kg of defatted canola meal was mixed with 510 kg ofwater in a tank. The pH of canola meal slurry was at about 6.0 andtemperature at 21° C. After holding for 1 hour and 50 minutes underagitation, the protein fraction was separated from wet solids using anAlfa Laval® decanter centrifuge at maximum g force.

The wet solids were mixed with 330 kg of water in a tank at ambienttemperature for 1 hour. This was followed by centrifugation using thedecanter to separate the washing extract from the washed solids.

The protein fractions were combined together and approximately 868 kg ofcombined protein fraction was produced. The combined protein fractionwas clarified using an Alfa Laval® disc stack centrifuge to remove theremaining insoluble solids. Approximately 67 kg of wet solids and 801 kgof clarified protein extract were produced, respectively.

801 kg of clarified protein extract was fed to a Alfa Laval UF® systemfitted with spiral wound membrane (2×GR60PP-3838/80, 6.08 m² totalsurface area) with a molecular weight cut-off of 25,000 Dalton. Shortlyafter the UF filtration was started at 40-43° C., a severe drop in fluxrate was observed, from 65 liters per square meter per hour to 11 litersper square meter per hour in 23 minutes. Approximately 50 g of phytase(Natuphos® 10,000 L Phytase) at 0.08% dosage based on the startingweight of defatted canola meal was added to the clarified proteinextract. The flux rate of UF filtration increased quickly from 11 litersper square meter per hour to 65 liters per square meter per hour. Theclarified protein extract was concentrated at 44-50° C. from the initial2.5% solids to 20% solids at an average flux rate of 41 liters persquare meter per hour using the Alfa Laval UF system. Purify of proteinextract was increased to 86% by ultrafiltration.

Discussion

Phytase broke phytates through enzymatic action, which prevented the gelformation of phytates-protein complex on the membrane surface. Thisresulted in higher average flux rate and increased the filtrationefficiency.

Example 17 Preparation of Canola Protein Isolate Using Phytase at HighpH

Approximately 55.5 kg of defatted canola meal was mixed with 444 kg ofwater in a tank. Approximately 50 g of phytase (Natuphos 10,000 LPhytase) at 0.09% dosage based on the starting weight of defatted canolameal was added to the canola meal slurry. The pH of canola meal slurrywas adjusted from 6.0 to 7.0 by addition of 6 M NaOH. The temperature ofcanola meal slurry was 25° C. After holding for 1 hour and 40 minutesunder agitation, the protein fraction was separated from wet solidsusing a Alfa Laval® decanter centrifuge at maximum g force.

The wet solids were mixed with 300 kg of water in a tank at ambienttemperature for 1 hour. This was followed by centrifugation using thedecanter to separate the washing extract from the washed solids.

The protein fractions were combined together and approximately 681 kg ofcombined protein extract was produced. The combined protein extract wasclarified using an Alfa Laval disc stack centrifuge to remove theremaining insoluble solids. Approximately 77 kg of wet solids and 604 kgof clarified protein extract were produced, respectively. The pH of theclarified protein extract was adjusted to 8.0 by addition of 6M NaOH.

604 kg of clarified protein extract at pH8.0 was fed to an Alfa Laval UFsystem fitted with spiral wound membrane (2×GR60PP-3838/80, 6.08 m²total surface area) with a molecular weight cut-off of 25,000 Dalton.The ultrafiltration temperature was controlled at 34-48° C. Severe dropin flux rate occurred from 53 liters per square meter per hour to 26liters per square per hour in 29 minutes. The pH of the clarifiedprotein extract was adjusted to 6.0, but no change in the flux rate ofUF filtration process was observed.

Discussion

Phytase has an optimum enzyme activity in the pH range of 3.0-6.0 andthe temperature range of 30-50° C. Phytase has little enzymatic activityabove a pH of 7.0-7.5. Therefore, phytase had no or little enzymeactivity in this trial due to a high pH of 7.0-8.0. Phytase might alsobe inactivated in high pH of 8.0.

Example 18 Preparation of Hydrolyzed Protein Concentrate from RecoveredFiber Solids

Approximately 126.3 kg of insoluble fiber solids were mixed with 100 kgof water in a tank. This was followed by pH adjustment to 8.3±0.1 using0.9 kg of 11.06% NaOH solution. Approximately 0.5 kg of a 1^(st)protease (Alcalase® 2.4 L FG) was added to the slurry. The slurry wasthen heated to 60±2° C. and held at this temperature for 4 hours. Theslurry was cooled down to 50±2° C. and pH adjusted to 6.5. Approximately0.5 kg of the 2^(nd) protease (Flavouzyme®) was added to the slurry,which was followed by holding at 50±2° C. for 4 hours. The slurry wascentrifuged using a Westfalia® Decanter at 3300×g to separate thehydrolyzed protein extract from the insoluble fiber fraction. Theinsoluble fiber was washed further with 120 kg of filtered tap water,which was again followed by centrifugation at 3300×g to separate thewash protein extract from the washed fiber solids using the Westfalia®Decanter. The hydrolyzed protein extract and the wash hydrolyzed proteinextract were combined. The combined hydrolyzed protein extract was fedto a Millipore® Ultrafiltration Unit (Model A60, Millipore Corporation,Bedford, Mass., USA) at ambient temperature. The Ultrafiltration Unit(UF) was fitted with three hollow fiber cartridges having a molecularweight cutoff of 10,000 daltons. Each cartridge contained 5 m² ofmembrane surface area. The hydrolyzed protein extract was pumped throughthe hollow fiber cartridges at a rate of 800-1000 kg/hr. The retentatewas recycled back to the feed tank and the permeate was collected inanother tank. The UF unit was operated at an inlet pressure of 25 psimaximum and a retentate back pressure of 15 psi maximum. The flux rateor permeate rate was about 190-300 kg/hr throughout the ultrafiltrationprocess. The ultrafiltration process continued until about 40 kg ofretentate remained in the feed tank. Approximately 260 kg of water wasadded continuously into the feed tank and ultrafiltration was conductedat ambient temperature using the same UF unit fitted with the same threehollow fiber cartridges. The original volume of retentate in the feedtank was held constant by adding water to make up for the removedpermeate. The retentate was recycled back to the feed tank. Theultrafiltration process continued until all 260 kg of water was added tothe retentate.

Approximately 540 kg of permeate and 47.7 kg of retentate were obtainedfrom the ultrafiltration process. The permeate was spray dried toproduce hydrolyzed protein concentrate using a Komline® Sanderson pilotplant spray dryer equipped with a centrifugal atomizer with a wheelspeed up to 10,000 rpm (Komline® Sanderson Ltd., Brampton, Ontario,Canada). The spray drying operation was conducted at an inlet airtemperature of 185±5° C. and an outlet air temperature of 85±5° C.Approximately 3.36 kg of spray dried hydrolyzed protein concentratecontaining 82% protein (dwb) was produced.

Example 19 Sedimentation Velocity Analysis of Protein Content of CanolaProtein Isolate, Protein Concentrate and Protein Hydrolyzate

Aliquots of each of a protein isolate, protein concentrate and a proteinhydrolyzate were dissolved in 3% NaCl at a weight concentration of 10 mgof powder per mL. After sitting overnight, a small portion of each wasdiluted 10-fold to make a solution for sedimentation velocity analysis.

Samples of the protein isolate, protein concentrate and proteinhydrolyzate were loaded into cells with 2-channel charcoal-eponcenterpieces with 12 mm optical pathlength. The 3% NaCl dilution bufferwas loaded into the reference channel of each cell. The loaded cellswere then placed into an AN-60Ti analytical rotor, loaded into aBecker-Coulter ProteomeLab® XL-I analytical ultracentrifuge equippedwith both absorbance and Rayleigh interference (refractive index)optical detection, and brought to 20° C. The rotor was then brought to3,000 rpm and the samples were scanned (using both absorbance scans andrefractive index scans) to confirm proper cell loading. The rotor wasthen brought to the final run speed of 55,000 rpm. Scans were recordedat this rotor speed approximately every 3.2 min for about 6.2 hours (114total scans for each optical system for each sample), and then the scanrate was dropped to every 20 minutes for an additional 15 hours (30additional scans). Only the refractive index scans were analyzed.

Discussion

The refractive index scans were analyzed using the c(s) method andanalysis program SEDFIT (version 11.3) (see Schuck, P. (2000),Size-distribution analysis of macromolecules by sedimentation velocityultracentrifugation and Lamm equation modeling, Biophys. J., 78,1606-1619, herein incorporated by reference). In this approach, many rawdata scans are directly fitted (about 195,000 data points for eachsample), to derive the distribution of sedimentation coefficients, whilemodeling the influence of diffusion on the data in order to enhance theresolution. The method works by assigning a diffusion coefficient toeach value of sedimentation coefficient based on an assumption that allspecies have the same overall hydrodynamic shape (with shape defined bythe frictional coefficient ratio relative to that for a sphere, f/f₀).The f/f₀ values were varied to find the best overall fir of the data foreach sample. A maximum entropy regularization probability of 0.683 (1σ)was used, and both time-dependent and radially-independent noise wereremoved. To convert the raw sedimentation coefficients to approximatestandardized values all proteins in the samples were assumed to have apartial specific volume of 0.73 mL/g. A density of 1.01919 g/mL andviscosity of 1.0503 cp at 20° C. were calculated for 3% NaCl using theprogram SEDNTERP (see Laue, T. M., Shah, B. D., Ridgeway, T. M., andPelletier, S. L. (1992) In: Analytical ultracentrifugation inbiochemistry and polymers and science, S. E. harding, A. J. Rowe, and J.C. Horton, eds. Royal Society of Chemistry, Cambridge, pp. 90-125,herein incorporated by reference).

The high-resolution sedimentation coefficient distributions for thecanola protein isolate and canola protein concentrate samples are shownin FIGS. 43 and 44, respectively. The graphs show a vertical axis givingthe concentration and the horizontal axis showing the separation on thebasis of sedimentation coefficient. Each distribution has beennormalized to account for any concentration differences among thesamples, by setting the total area under the curve to 1.0 (100%) so thearea for each peak gives the fraction of that species. The sedimentationcoefficients have been approximately converted to standard conditions(adjusted for the fact that the density and viscosity of 3% NaCl aregreater than those for pure water). This conversion is approximatebecause the information needed to make a precise buoyancy correction foreach individual component is not known, and therefore a typical value isused for all components (the as-measured raw sedimentation coefficientswere multiplied by 1.1108 to convert to s_(20,w) values).

The protein isolate had the following percentages of proteins: 0.75S(9.6% w/w), 1.7S (16.7%), 2.9S (1.8%), 4.6S (1.2%), 6.5S (2.6%), 7.7S(0.5%), 9.6S (0.3%), 12.3S (56.7%), 15.1S (2.4%), 18.5S (5.6%) and 22S(2.8%) as shown in FIG. 43.

The protein concentrate had the following percentages of proteins: 1.7S(51.9% w/w), 2.7S (4.1%), 3.4S (1.1%), 5.3S (0.9%), 6.9S (1.1%), 7.9S(0.1%), 9.3S (0.1%), 12.3S (36.5%), 15.6 S (1.2%), 18.1S (2.2%) and 22S(0.8%) as shown in FIG. 44.

The hydrolyzed protein concentrate had the following percentages ofproteins: 0.78S (8.9% w/w), 3.1S (0.97%), 4.4S (0.15%), 6.7S (0.04%),7.9S (0.03%), 9.5S (0.16%), 11.4S (0.32%), 14.1S (0.38%) and 16.1S(0.15%) as shown in FIG. 45.

The size distribution for the canola protein isolate is shown in FIG.44, possessing a total of 92.8% protein on a dry weight basis. The maincomponent (largest fraction weight) is a species at 12.3S which is 56.7%of the total, which corresponds to a 12S protein. The two next mostabundant species are at 1.7S (16.7%) (corresponding to “2S” protein) and0.75S (9.6%) (which could also correspond to “2S” protein). Fiveadditional minor peaks or shoulders occur between those species and themain 12.3S peak, and three other peaks sedimenting faster than the mainpeak. There is also a peak at 22.2S, it is possible that some or all ofthis 2.8% is actually sedimenting faster than 22.2S. It is also possiblethat the isolate sample contained some very large aggregates orincompletely-dissolved components that pelleted during the rotoracceleration to 55,000 rpm and therefore were not detected.

The results for the canola protein concentrate sample are shown in FIG.44, possessing a total of 71.2% protein on a dry weight basis. Theprotein concentration (total signal) of this sample is more than 2-foldlower than that of the protein isolate, presumably due to loss ofinsoluble material. In this case the principal component is the peak at1.7S (corresponding to a “2S” protein), which is 51.9% of the total,with the 12S protein still a major component (36.5%). This samplecontains little of a 7S component. It is important to note thatequivalent peaks will not necessarily appear at exactly the samesedimentation coefficient. With this method it is normal for thepositions of minor peaks to shift somewhat from one sample toanother—the sedimentation coefficients for species at levels of a fewpercent or less cannot be determined with high precision (there is noiseon the x-axis).

The results for the hydrolyzed canola protein sample are shown in FIG.45, possessing a total of 82% protein on a dry weight basis. Thenormalization to give percentages of the total was handled differentlyfor this sample, as it was not possible to measure the total signal forthis sample because some of the peptide fragments are so small that evenafter over 21 hr at 55,000 rpm they have not sedimented sufficiently todeplete the concentration to zero at the inner regions of the cell.Therefore the total signal was estimated based on the weightconcentration (1 mg of powder per mL), a peptide content for the powderof 82% by weight, and the nominal detector sensitivity of 3.3±0.1fringes per (mg/mL). The vertical scaling in FIG. 43 is identical tothat for FIG. 44. Therefore in FIG. 44 the area under each peak measuresthe fraction of that protein species remaining after hydrolysis(fraction of the total, not fraction of that individual species), andthe total area under the curve is less than 100%. The actual total areais 12.0% (that is, peptides or proteins that are still large enough tosediment significantly represent 12.0% of the total expected signal).Note that the peak at 0.78S represents nearly three-fourths of thattotal of 12.0%, and this peak could represent a fragment of one of thelarger proteins. Because the areas for many of the other peaks in thissample are so small the ones below 1% are listed to the nearest 0.01% tolimit the round-off error. The peak at 1.7 S was not detected in thissample. The peak at 11.4 S (0.32%) may represent a partially-digested(clipped) form of the 12.3 S species; whether or not that is correct, itis clear that species at 11-13 S are at least 100-fold less abundantthan in FIGS. 43 and 44.

TABLE 1 Heat Treatment Conditions Heat Treatment Temperature (° C.)Residence Time 1 75 15 seconds 2 80 15 seconds 3 85 15 seconds 4 85 15seconds 5 85 15 seconds 6 90 15 seconds Control 95 30 minutes

TABLE 2 Heat Treatment Conditions Heat Treatment Temperature (° C.) Time(second.) 1 100 15 2 105 15 3 110 15 4 120 15 5 130 15

TABLE 3 Evaluation of Heat Treatments on Quality of Defatted Canola Meal(B. juncea) Protein of Oil of Heat Moisture of PDI of Defatted DefattedTreatment Defatted Meal Defatted Meal Meal Conditions (%) Meal (%, asis) (%, as is)  75° C. for 15 7.81 34.43 41.3 2.08 Seconds.  80° C. for15 7.30 34.17 43.2 1.54 Seconds.  85° C. for 15 11.56 31.55 41.3 4.03Seconds  90° C. for 15 7.54 31.98 43.0 1.29 Seconds  95° C. for 15 7.8231.97 41.9 1.47 Seconds 100° C. for 15 7.50 30.33 40.2 1.74 Seconds 105°C. for 15 7.79 29.32 39.0 1.99 Seconds 110° C. for 15 7.67 27.82 37.71.64 Seconds 120° C. for 15 7.11 23.10 33.7 1.58 Seconds 130° C. for 157.19 18.20 28.6 1.66 Seconds No Heat 10.37 31.92 39.2 5.31 TreatmentHeat 8.03 32.22 42.6 2.78 Treatment at  95° C. for 0.5 Hr.

TABLE 4 Evaluation of Heat Treatment on the Sulphur Content of Pressedand Extracted Canola Oils (B. juncea) Sulphur in Sulphur in Sulphur inbutane/R134a Methyl Pentane Heat Treatment Pressed Oil Extracted OilExtracted Oil Conditions (ppm) (ppm) (ppm)  75° C. for 15 Seconds. 21.599.3 222  80° C. for 15 Seconds. 9.77 101 175  85° C. for 15 Seconds9.82 562 111  90° C. for 15 Seconds 9.67 86.4 55.3  95° C. for 15Seconds 8.71 75.8 34.5 100° C. for 15 Seconds 8.65 71.4 not determined105° C. for 15 Seconds 7.13 61.8 not determined 110° C. for 15 Seconds8.94 55.8 not determined 120° C. for 15 Seconds 8.77 48.7 not determined130° C. for 15 Seconds 9.82 19.9 not determined No Heat Treatment 46.9303 205 Heat Treatment at 41.8 254 98.3  95° C. for 0.5 Hr.

TABLE 5 Evaluation of Heat Treatment on the FFA Content of Pressed andExtracted Canola Oils (B. juncea) FFA in FFA in Methyl FFA inbutane/R134a Pentane Heat Treatment Pressed Oil Extracted Oil ExtractedOil Conditions (%) (%) (%)  75° C. for 15 1.67 2.48 2.70 Seconds.  80°C. for 15 1.70 2.35 2.40 Seconds.  85° C. for 15 Seconds 1.67 2.61 2.48 90° C. for 15 Seconds 1.65 2.06 2.39  95° C. for 15 Seconds 1.60 2.222.38 100° C. for 15 1.26 2.07 not determined Seconds 105° C. for 15 1.382.12 not determined Seconds 110° C. for 15 1.23 2.13 not determinedSeconds 120° C. for 15 1.37 1.94 not determined Seconds 130° C. for 151.33 2.15 not determined Seconds No Heat Treatment 1.67 2.47 2.72 HeatTreatment at 1.67 2.63 2.78  95° C. for 0.5 Hr.

TABLE 6 Evaluation of Heat Treatment on the Phosphorus Content ofPressed and Extracted Canola Oils (B. juncea) Phosphorus Phosphorus inPhosphorus in in Pressed butane/R134a Methyl Pentane Heat Treatment OilExtracted Oil Extracted Oil Conditions (ppm) ppm) (ppm)  75° C. for 15not 2.93 1020  Seconds. determined  80° C. for 15 not 2.65 899 Seconds.determined  85° C. for 15 Seconds not 8.43 975 determined  90° C. for 15Seconds not 2.72 735 determined  95° C. for 15 Seconds not 22.8  805determined 100° C. for 15 36.2 not determined not determined Seconds105° C. for 15 26.3 not determined not determined Seconds 110° C. for 1531.8 not determined not determined Seconds 120° C. for 15 117   notdetermined not determined Seconds 130° C. for 15 30.3 not determined notdetermined Seconds No Heat Treatment not 4.25 962 determined HeatTreatment at not not determined 875  95° C. for 0.5 Hr. determined

TABLE 7 Analytical Results of Pressed Canola Cakes (B. juncea) Moistureof Oil Content of Press Cake Press Cake Sample (%) (%) 75° C. for 15Seconds. 11.4 26.2 80° C. for 15 Seconds. 10.4 27.6 85° C. for 15Seconds 10.2 24.4 90° C. for 15 Seconds 9.00 27.9 95° C. for 15 Seconds9.46 26.9 100° C. for 15 Seconds 8.20 28.0 105° C. for 15 Seconds 7.6022.7 110° C. for 15 Seconds 9.01 23.5 120° C. for 15 Seconds 8.60 37.7130° C. for 15 Seconds 6.15 22.1 No Heat Treatment 12.0 26.4 HeatTreatment at 95° C. 12.1 24.6 for 0.5 Hr.

TABLE 8 Analysis of Defatted Meal, Protein-Enriched Meal and 65% ProteinConcentrate Carbo- Protein Ash Crude Oil hydrates Moisture (%, (%, Fiber(% (%, Sample (%) dwb) dwb) (%, dwb) dwb) dwb) Canola Seed 6.25 27.244.1 4.52 42.27 21.87 (b. juncea) Pressed Cake 8.2 33.66 5.23 5.2 30.525.41 Defatted Meal 7.5 43.36 7.29 6.99 1.88 40.38 Protein 6.76 52.447.47 4.37 1.56 34.16 Enriched Meal Fiber Enrich 7.47 43.01 6.94 9.832.44 37.78 Meal Protein 4.55 64.74 8.23 5.77 0.55 20.71 ConcentrateDried Sugar 6.43 12.40 5.75 0.17 1.93 79.75 Fraction

TABLE 9 Water Addition and Seed Weight for Each Batch of MoistureAdjustment and Mixing Weight of Amount of Mixing Canola Seed Water AddedTime Batch (kg) (kg) (Min.) 1 220.5 4.41 5 2 221.0 4.42 5 3 221.0 4.42 54 222.0 4.44 5 5 223.5 4.47 5 6 225.0 4.50 5 7 221.0 4.42 5 8 225.0 4.505 9 211.0 4.22 5 10 224.5 4.49 5 11 222.0 4.44 5 12 220.5 4.41 5 13214.0 4.28 5 14 47.5 0.95 5 Total 2918.5 53.96

TABLE 10 Mass Balance of Flaking and Pressing Trials Canola Flaked PressRatio of Seed Seed Cake Press Oil Cake/ Sample (kg) (kg) (kg) (kg) SeedSample 1a 300.5 NA 181.6 73.1 60.43 Sample 1b 2,676 2,676 1,566 87258.52

TABLE 11 Results of Proximate Analysis for Canola Seed and Press CakesCanola Seed (moisture adjusted) Sample 1a Sample 1b Moisture (%) 8.127.62 10.33 Protein (%, dwb^(a)) 27.00 34.86 42.04 Crude Oil (%, dwb^(a))44.39 32.37 12.58 Crude Fiber (%, dwb^(a)) 4.75 5.3 7.00 Ash (%,dwb^(a)) 4.56 4.87 7.02 ^(a)dwb = dry weight basis

TABLE 12 The Results of Screening Trials for Lab and Milled Canola MealsScreening Trial Sample 1e Sample 1f Milled Canola Meal (%, w/w) (%, w/w)1 57.23 42.76 2 47.05 52.94 3 42.33 57.66 4 49.49 50.51 5 49.29 50.71 643.96 56.04 7 46.89 53.11 8 47.16 52.84 Average 47.93 52.07 Milling andScreening - 42.85 57.15 Sample 2b Milling and Screening- 40.31 59.69Sample 3b Screening Trial - Sample 1 37.14 62.86

TABLE 13 Processing Conditions for Samples 1-3 of Press Cakes, ExtractedMeals, Fiber Enriched Meals and Protein Concentrates Sample 1 Sample 2Sample 3 Canola Seed B. juncea B. juncea B. juncea Flaking Yes No NoTemperature of Heat 75-96° C. N/A N/A Treatment in Cooker Residence Timein 20 minutes 30 minutes 30 minutes Cooker Press Cake 68-79° C. NA NATemperature Extraction of Press Butane/R134a Butane/R134a Butane/R134aCake Temperature for Room Room Room Milling and Temperature TemperatureTemperature Screening of (23° C.) (23° C.) (23° C.) Defatted MealsExtraction of Room Room Room Protein Enriched Temperature TemperatureTemperature Meals (23° C.) (23° C.) (23° C.) 80% (v/v) ethanol 80% (v/v)ethanol 80% (v/v) Three Three Extractions ethanol Extractions (ratio(ratio of 1 to 6 by Three of 1 to 6 by weight of meal to Extractions(ratio weight of meal to ethanol) of 1 to 6 by ethanol) weight of mealto ethanol) Temperature and 54 ± 3° C. for 18 Room Room Residence Timefor hours in a Temperature Temperature Desolventization Vacuum Dryer(23° C.) in a Fume (23° C.) in a Fume and Drying of Hood for 3 days Hoodfor 3 days Protein 50° C. in a 50° C. in a Concentrates Vacuum Dryer forVacuum Dryer 15 Hours for 15 Hours Milling and Room Room Room ScreeningTemperature Temperature Temperature (23° C.) (23° C.) (23° C.)

TABLE 14 Moisture and Oil Contents of Samples 1a-d Moisture Crude OilContent Content Sample Mass of Run (%) (%, dwb^(a)) Sample 1a 1 kg 9.3226.81 Sample 1c 1 kg 6.13 8.75 Sample 1b 1 kg 8.58 15.12 Sample 1d 1 kg5.81 1.94 Sample 1b 9 kg 8.00 27.83 Sample 1d 9 kg 5.38 12.73 ^(a)dwb =dry weight basis

TABLE 15 Moisture and Oil Contents of Press Cake from Flaking Trial(Sample 1b) Moisture Crude Oil Content Content Sample Mass of Run (%)(%, dwb^(a)) Sample 1b 8.9 kg 7.73 13.94 Sample 1b 8.9 kg 7.25 14.00Sample 1b 8.9 kg 7.38 15.03 Sample 1b 8.9 kg 7.22 17.68 Sample 1b 8.9 kg6.90 22.90 Sample 1b 8.9 kg 7.05 19.68 Sample 1b 8.9 kg 7.30 19.77Sample 1b 8.9 kg 7.70 19.92 Sample 1b 8.9 kg 7.85 19.01 Sample 1b 8.9 kg8.02 14.68 Flaked Juncea NA 9.13 13.76 Press Cake Composite (MultipleRuns) Flaked Juncea NA 9.04 13.52 Press Cake Composite (Multiple Runs)Sample 1b   9 kg 8.42 13.03 Sample 1b   9 kg 8.26 13.04 Sample 1b   9 kg6.63 13.33 Sample 1b 8.9 kg 8.32 13.46 Sample 1b 8.9 kg 8.36 13.65Sample 1b 8.9 kg 8.35 13.73 Sample 1b 8.9 kg 8.57 12.96 Sample 1b 8.9 kg8.58 12.92 Sample 1b 8.9 kg 8.40 12.72 Sample 1b 8.9 kg 8.00 13.06Sample 1b 8.9 kg 7.14 17.21 Sample 1b 8.9 kg 7.29 16.80 Sample 1b 8.9 kg7.20 14.26 Flaked Juncea NA 7.97 13.22 Press Cake Composite (MultipleRuns) Flaked Juncea NA 8.49 14.38 Press Cake Composite (Multiple Runs)Flaked Juncea NA 8.09 14.07 Press Cake Composite (Multiple Runs) FlakedJuncea NA 7.41 16.64 Press Cake Composite (Multiple Runs) Flaked JunceaNA 7.95 14.92 Press Cake Composite (Multiple Runs) Flaked Juncea NA 8.3315.86 Press Cake Composite (Multiple Runs) Flaked Juncea NA 7.1 14.90Press Cake Composite (Multiple Runs) Flaked Juncea NA 7.68 13.91 PressCake Composite (Multiple Runs) Flaked Juncea NA 8.47 14.18 Press CakeComposite (Multiple Runs) ^(a)dwb = dry weight basis

TABLE 16 Moisture and Oil Contents of Sample 1d Moisture Crude OilContent Content Sample Mass of Run (%) (%, dwb^(a)) Sample 1d 8.9 kg4.81 1.70 Sample 1d 8.9 kg 4.14 1.76 Sample 1d 8.9 kg 6.53 2.3 Sample 1d8.9 kg 6.44 2.45 Sample 1d 8.9 kg 6.54 2.63 Sample 1d 8.9 kg 6.18 1.89Sample 1d 8.9 kg 5.80 2.49 Sample 1d 8.9 kg 6.33 2.93 Sample 1d 8.9 kg6.10 2.85 Sample 1d 8.9 kg 6.02 2.14 Sample 1d 8.9 kg 5.61 2.26 FlakedJuncea — 8.70 2.36 Extracted Meal Composite (Multiple Runs) FlakedJuncea — 8.27 2.30 Extracted Meal Composite (Multiple Runs) FlakedJuncea   9 kg 8.20 2.68 Extracted Meal Composite (Multiple Runs) FlakedJuncea   9 kg 8.38 2.13 Extracted Meal Composite (Multiple Runs) FlakedJuncea   9 kg 7.13 2.27 Extracted Meal Composite (Multiple Runs) FlakedJuncea   9 kg 7.74 2.03 Extracted Meal Composite (Multiple Runs) Sample1d   9 kg 6.44 2.63 Sample 1d   9 kg 6.28 2.50 Sample 1d   9 kg 6.543.13 Flaked Juncea — 7.40 2.79 Extracted Meal Composite (Multiple Runs)Flaked Juncea — 7.79 2.51 Extracted Meal Composite (Multiple Runs)Flaked Juncea — 8.18 2.47 Extracted Meal Composite (Multiple Runs)Flaked Juncea — 6.46 2.44 Extracted Meal Composite (Multiple Runs)Flaked Juncea — 6.84 2.78 Extracted Meal Composite (Multiple Runs)Flaked Juncea — 8.03 1.87 Extracted Meal Composite (Multiple Runs)Flaked Juncea — 6.70 2.70 Extracted Meal Composite (Multiple Runs)Flaked Juncea — 6.39 1.79 Extracted Meal Composite (Multiple Runs)Flaked Juncea — 7.06 2.02 Extracted Meal Composite (Multiple Runs)^(a)dwb = dry weight basis

TABLE 17 Results of Proximate Analysis for Juncea Seed and Samples 1b,1d-g, 2a-d and 3a-d Crude Crude Protein Oil Ash Fiber Moisture (%, (%,(%, (%, Sample (%) dwb^(a)) dwb^(a)) dwb^(a)) dwb^(a)) PDI Canola Seed8.12 27.00 44.39 4.56 4.75 25.64 (B. juncea) Sample 1b 10.33 42.04 12.587.02 7.00 28.78 Sample 1d 6.86 47.02 1.38 8.12 7.75 33.35 Sample 2a 6.5649.98 0.92 7.12 7.63 33.04 Sample 3a 6.99 47.31 2.29 6.61 7.60 28.42Sample 1f 6.18 46.10 2.48 6.86 8.28 31.91 Sample 2c 6.60 46.25 1.48 6.909.79 29.41 Sample 3c 6.73 44.39 3.18 6.45 8.60 29.33 Sample 1e 6.9053.92 1.49 7.07 5.03 — Sample 2b 6.16 54.77 0.51 7.06 5.49 — Sample 3b6.50 52.62 1.37 6.67 4.82 — Sample 1g 5.51 65.80 0.41 8.03 7.16 — Sample2d 5.52 68.69 0.02 8.1 7.11 — Sample 3d 5.32 69.60 0.31 7.68 6.37 —^(a)dwb = dry weight basis

TABLE 18 Yields of Protein Concentrates Weight of Weight of ProteinProtein Yield of Protein Enriched Meal Concentrate Concentrate Sample(kg) (kg) (%) 1g 412 (Sample 1e) 248.3 60.27 2d 1.5 (Sample 2b) 1.173.33 3d 3.9 (Sample 3b) 2.38 61.03

TABLE 19 Analytical Results of Sample 2d Moisture 4.86% (as is) GrossFat 0.28% (as is) Gross Protein 65.0% (as is) Gross Ash 7.00% (as is)Gross Fiber 6.30% (as is) Carbohydrate 16.56% (as is) Starch 0.56% (asis) Total Glucosinolate 0.500 μmole/g Phytic Acid 732 (mg/kg) PhyticBounded Phosphorus 206 (mg/kg)

TABLE 20 Amino Acid Profile (Acid Hydrolysis) of Sample 2d Alanine 3.18(g/100 g) Arginine 4.89 (g/100 g) Aspartic Acid 5.74 (g/100 g) GlutamicAcid 10.6 (g/100 g) Glycine 3.67 (g/100 g) Histidine 1.82 (g/100 g)Isoleucine 2.84 (g/100 g) Leucine 5.23 (g/100 g) Lysine 3.28 (g/100 g)Phenylalanine 2.87 (g/100 g) Proline 3.30 (g/100 g) Serine 3.06 (g/100g) Threonine 3.10 (g/100 g) Tyrosine 2.35 (g/100 g) Valine 3.46 (g/100g) Tryptophan 0.927 (g/100 g)  Cystein + Cystine 1.02 (g/100 g)Methionine 1.23 (g/100 g)

TABLE 21 Glucosinolate Profile of Samples 1g, 2d and 3d on a Dry WeightBasis Sample 1g Sample 2d Sample 3d Total Glucosinolates 3.81 6.85 0.46(μmole/g) allyl — 0.06 — 3-butenyl 1.41 2.36 0.20 4-pentenyl 0.06 0.11 —2-OH-3-butenyl — 0.13 — 2-OH-4-pentenyl — — — CH3-thiopentenyl — — —phenylethyl — — — CH3-thiopentenyl — — — 3-CH3-indolyl — — —4-OH-3-CH3-indolyl 2.34 4.18 0.26 Total Aliphatic 1.52 2.59 0.22Glucosinolates

TABLE 22 Glucosinolate Profile of 1d, 2a and 3a on a Dry Weight BasisSample 1d Sample 2a Sample 3a Total Glucosinolates 20.93 20.87 18.60(μmole/g) allyl 0.27 0.29 0.26 3-butenyl 14.26 14.23 12.70 4-pentenyl0.84 0.83 0.72 2-OH-3-butenyl 0.88 0.90 0.76 2-OH-4-pentenyl — — —CH3-thiopentenyl 0.03 0.09 — phenylethyl 0.18 0.19 0.14 CH3-thiopentenyl0.05 0.05 — 3-CH3-indolyl 0.11 0.11 0.13 4-OH-3-CH3-indolyl 2.29 4.183.89 Total Aliphatic 15.97 15.96 14.18 Glucosinolates

TABLE 23 Sinapine and Phytate Contents in Samples 1g, 2d and 3d andSamples 1d, 2a and 3a on an As Is Basis Sample 1g Sample 2d Sample 3dSinapine (phenyl 0.006 0.003 0.007 propanoid) % (as is) Total PhyticAcid 3.18  2.71 ± 0.029  3.35 ± 0.039 % (as is) Sample 1d Sample 2aSample 3a Sinapine (phenyl 0.122 0.239 0.104 propanoid) % (as is) TotalPhytic Acid 2.53 ± 0.10 2.56 ± 0.15 2.59 ± 0.13 % (as is)

TABLE 24 Solvent Residues in 1, 2a and 2c Before Vacuum Drying SampleSolvent Residues 1 Butane: 160 ppm and R134a: 435.2 ppm 2a Butane: 194ppm and R134a: 1414.3 ppm 2c Butane: 178 ppm and R134a: 1049.3 ppm

TABLE 25 Solvent Residues in Samples 1-3 after Desolventization andDrying in a Vacuum Dryer at 50° C. for 15 Hours. Sample 1 Sample 2Sample 3 Sample 1d, Butane: <10 ppm Butane: 16.8 ppm Butane: 11 ppm 2aand 3a R134a: <10 ppm R134a: 41.5 ppm R134a: <10 ppm Sample 1f, Butane:<10 ppm Butane: 15 ppm Butane: <10 ppm 2c and 3c R134a: <10 ppm R134a:41.7 ppm R134a: <10 ppm Sample 1g, Ethanol: 32.8 ppm Ethanol: NAEthanol: 6.6 ppm 2d and 3d Ethyl Acetate: Ethyl Acetate: Ethyl Acetate:<1.0 ppm <1.0 ppm <1.0 ppm Butane: <10 ppm Butane: <10 ppm Butane: <10ppm R134a: <10 ppm R134a: <10 ppm R134a: <10 ppm

TABLE 26 Results of the Proximate Analysis for Canola Seed, Canola SeedPress Cake, Defatted Meal, Protein Enriched Meal, Fiber Enriched Meal,Canola Protein Concentrate, Hydrolyzed Canola Protein Concentrate andCanola Protein Isolate. Protein Crude Moisture (%, Ash Oil Fiber Sample(%) dwb^(a)) (%, dwb^(a)) (%, dwb^(a)) (%, dwb^(a)) Canola Seed 8.1227.0 4.56 44.39 4.75 Canola Seed 10.33 42.0 7.02 12.58 7.00 Press cakeDefatted Meal 6.86 47.0 8.12 1.38 7.75 Protein 6.71 52.0 8.34 0.84 5.53Enriched Meal Fiber Enriched 6.91 43.6 7.88 1.29 9.00 Meal Protein 6.1470.6 10.5 0.11 4.88 Concentrate Hydrolyzed 6.44 88.8 5.98 0.24 0.00Protein Concentrate Protein Isolate 3.90 92.8 3.54 0.04 0.00 ^(a)dwb =dry weight basis

TABLE 27 Results of Proximate Analysis on Samples for Production ofProtein Concentrate Having About 70% Protein Crude Solids MoistureProtein Ash Oil Fiber Sample (%) (%) (%, dwb) (%, dwb) (%, dwb) (%, dwb)Bird Decanter - 15.42 4.19 47.5 8.42 0.66 10.2 Canola fiber 1^(st) passBird Decanter - 15.33 4.81 45.4 0.69 12.7 Washed Canola fiber 2^(nd)pass Bird Decanter - 8.26 10.3 52.4 10.16 0.06 3.20 Protein slurry afterfiber removal Bird Decanter - 4.80 7.37 49.6 9.61 0.42 6.52 Proteinslurry after fiber removal 2^(nd) pass Westfalia decanter - 19.54 7.3552.6 10.81 0.21 6.89 Protein solids #1 Westfalia decanter - 3.75 — —7.29 — — Protein Extract #1 Westfalia decanter - 15.74 6.59 48.4 11.490.14 9.92 Protein solids #2 Westfalia decanter - 1.65 — — — — — Proteinextract #2 Disc stack centrifuge - 15.72 — — — — — Protein solids Discstack centrifuge - 2.61 — — — — — Clarified protein extract Permeate -1.14 — — — — — Ultrafiltration Permeate - 0.19 Diafiltration Proteinretentate - 13.17 6.90 90.4 2.14 0.12 0.00 Ultrafiltration (UF) Proteinretentate - 3.40 1.34 92.4 2.65 0.01 0.03 Diafiltration (DF) Proteinisolate 5.50 — — — — — solution - UF and DF Westfalia decanter - 2.27 —75.0 — — — hydrolyzed protein extract 1 Westfalia decanter - 12.98 5.8927.8 18.1 2.53 14.5 canola fiber solids #1 Westfalia decanter - 1.12 —58.5 — — — hydrolyzed protein extract 2 Westfalia decanter - 11.74 5.8419.6 18.8 2.28 21.4 canola fiber solids - 2^(nd) centrifuge

TABLE 28 Amino Acid Profiles of Protein Concentrate, Hydrolyzed ProteinConcentrate and Protein Isolate on a Dry Weight Basis Hydrolyzed ProteinProtein Protein Amino Acid Concentrate Concentrate Isolate Aspartic Acid(%, dwb^(a)) 4.84 7.05 7.91 Glutamic Acid (%, dwb^(a)) 12.25 15.71 17.48Serine (%, dwb^(a)) 3.61 4.63 4.45 Glycine (%, dwb^(a)) 3.82 4.58 5.13Histidine (%, dwb^(a)) 1.71 2.20 2.19 Arginine (%, dwb^(a)) 5.79 7.416.92 Threonine (%, dwb^(a)) 3.18 4.35 3.74 Alanine (%, dwb^(a)) 3.484.90 4.56 Proline (%, dwb^(a)) 4.07 5.70 5.22 Tyrosine (%, dwb^(a)) 2.775.10 3.28 Valine (%, dwb^(a)) 3.79 4.77 4.95 Methionine (%, dwb^(a))1.40 1.75 2.02 Cystine (%, dwb^(a)) 1.17 1.46 1.55 Isoleucine (%,dwb^(a)) 3.18 4.75 4.06 Leucine (%, dwb^(a)) 5.76 6.38 7.36Phenylalanine (%, dwb) 3.34 3.62 4.23 Lysine (%, dwb^(a)) 3.77 5.55 4.10Tryptophan (%, dwb^(a)) 1.02 1.09 1.38 Total Amino Acid (%, 68.95 91.0090.53 dwb^(a)) ^(a)dwb = dry weight basis

TABLE 29 Amino Acid Profiles of Canola Protein Concentrate, HydrolyzedCanola Protein Concentrate, Canola Protein Isolate, Soy Protein Isolateand Pea Protein Isolate on a Normalized Basis of Pure Protein HydrolyzedCanola Canola Canola Soy Pea Protein Protein Protein Protein ProteinAmino Acid Concentrate Concentrate Isolate Isolate Isolate Aspartic Acid7.02 7.75 8.74 11.5 11.78 (%) Glutamic Acid 17.77 17.26 19.31 19.0 19.13(%) Serine (%) 5.24 5.09 4.92 5.2 5.28 Glycine (%) 5.54 5.03 5.67 4.13.86 Histidine^(a) (%) 2.48 2.42 2.42 2.6 2.55 Arginine (%) 8.40 8.147.64 7.5 8.58 Threonine^(a) (%) 4.61 4.78 4.13 3.8 3.68 Alanine (%) 5.055.39 5.04 4.2 4.15 Proline (%) 5.90 6.26 5.77 5.1 4.15 Tyrosine (%) 4.025.60 3.62 3.8 3.68 Valine^(a) (%) 5.50 5.24 5.47 5.0 4.90 Methionine^(a)2.03 1.92 2.23 1.3 1.13 (%) Cystine (%) 1.70 1.60 1.71 1.3 1.04Isoleucine^(a) (%) 4.61 5.22 4.49 4.8 4.43 Leucine^(a) (%) 8.35 7.018.13 8.1 8.20 Phenylalanine^(a) 4.84 3.98 4.67 5.2 5.29 (%) Lysine^(a)(%) 5.47 6.10 4.53 6.2 7.26 Tryptophan^(a) 1.49 1.20 1.52 1.3 0.94 (%)Total Amino 100 100 100 100 100 Acid (%) ^(a)Nine essential amino acids.

TABLE 30 Essential Amino Acid Profiles of Canola Protein Concentrate,Hydrolyzed Canola Protein Concentrate, Canola Protein Isolate, SoyProtein Isolate and Pea Protein Isolate and Their Functions on HumanNutrition Specific Hydrolyzed Benefit and Canola Canola Canola Soy PeaImpact on Amino Protein Protein Protein Protein Protein Human AcidConcentrate Concentrate Isolate Isolate Isolate Nutrition Histidine (%)2.48 2.42 2.42 2.6 2.55 — Threonine 4.61 4.78 4.13 3.8 3.68 BrainActivity (%) Valine^(a) (%) 5.50 5.24 5.47 5.0 4.90 Muscle MassMethionine 2.03 1.92 2.23 1.3 1.13 Muscle (%) Building, Antioxidant andDevelopment of Appendages Isoleucine 4.61 5.22 4.49 4.8 4.43 Muscle Mass(%) Leucine (%) 8.35 7.01 8.13 8.1 8.20 Muscle Mass Phenylalanine 4.843.98 4.67 5.2 5.29 — (%) Lysine (%) 5.47 6.10 4.53 6.2 7.26 GrowthTryptophan 1.49 1.20 1.52 1.3 0.94 Sleep Aid (%) and Anti- depression

TABLE 31 Functional Properties of Canola Protein Isolate as Compared toSoy and Pea Protein Isolates Concentration Emulsifying Emulsion FoamingFoam of Protein Capacity at Stability Capacity Stability Isolate pH 7 atpH 7 at pH 7 at pH 7 Sample (%, w/w) (%) (%) (%) (%) Canola 0.5 58 55352 18.5 Protein 1.0 66 60 389 26 Isolate Soy 0.5 59 57 108 4.9 Protein1.0 64 60 478 21 Isolate Pea 0.5 57 52 24.4 7 Protein 1.0 62 58 202 7Isolate

TABLE 32 Functional Properties of Canola Protein Isolate FunctionalProperty Results and Comments Emulsifying Capacity Emulsifying capacityof 0.5% canola protein isolate solution was high, comparable to that of5% native egg yolk. Emulsion of Canola Protein Oil Content of EmulsionIsolate 50.0 Stable 60.0 Stable 70.0 Stable 72.5 Stable 75.0 Stable 77.5Instable Foaming and Foam Foaming properties of canola protein isolateStability were superior in comparison to whey protein isolate as shownin FIG. 36. Foam Volume (mL) Heated at 60° for 15 minutes and then FoamVolume cooled to (mL) 20° C., finally Whipping at whipping at 20° C. for1 20° C. for 1 Time (min) minute minute  0 80 75  5 61 59 10 60 58 15 5856 30 53 50 45 52 42 60 50 38 Gel Formation and Gel Canola proteinisolate required higher Strength temperature for gel formation incomparison to whey protein isolate, as shown in FIGS. 37 and 38 Gelfirmness of canola protein isolate was comparable to that of wheyprotein isolate and soy protein isolate gels at 5% protein content. Forcanola protein isolate, gels with 7% protein content were strong, gelswith 3-5% content possessed a medium scaled strength, and gels with 2%protein content were very weak, as shown in FIG. 39. WaterImmobilization Water immobilization of canola protein isolate gels wasslightly lower than that of whey protein isolate gels.

TABLE 33 Results of Solubility Tests on Canola, Pea and Soy ProteinIsolate Solubility Test Method Borate-phosphate buffer (12.20 g/L ofNaH₂PO₄•H₂O and 8.91 g/L of Na₂B₄O₇•10H₂O) 1% concentration pH 6.7 39°C. 1 hour Solubility of Canola 99.81 Protein Isolate (%, w/w) (Obtainedfrom Example 5 (b)) Solubility of Pea Protein 18.85 Isolate (%, w/w)Solubility of Soy Protein 25.21 Isolate (%, w/w)

TABLE 34 Anti-nutritional Factors of Canola Protein IsolateAnti-nutritional Factors Content Total Glucosinolate 0.200 μmol/g ErucicAcid 0.1% of total fat (1.7% total fat) Phytic Acid <0.05% PhyticBounded <0.01% Phosphorus Allyl Isothiocyanate <0.02%

TABLE 35 Glucosinolates in Juncea Seed, Press Cake. BioExx ExtractedMeal, Protein Enriched meal, Fiber Enriched Meal, Protein Concentrate,Hydrolyzed Protein Concentrate, and Protein Isolate BioExx ProteinJuncea Extracted Enriched Glucosinolates Seed Press Cake Meal Meal Allyl0.12 0.21 0.25 0.26 (μmoles/g) 3-butenyl 6.69 10.34 12.23 14.71(μmoles/g) 4-pentenyl 0.46 0.72 0.85 0.99 (μmoles/g) 2-OH-3-butenyl 0.761.18 1.40 1.58 (μmoles/g) CH3-thiobutenyl 0 0.05 0.05 0.05 (μmoles/g)Phenylethyl 0.17 0.27 0.32 0.37 (μmoles/g) 3-CH3-indolyl 0.48 0.81 0.911.01 (μmoles/g) 4-OH-3-CH3- 2.11 2.95 3.56 4.20 indolyl (μmoles/g) TotalAliphatics 7.92 12.26 14.51 17.31 (μmoles/g) Fiber Canola HydrolyzedCanola Enriched Protein Protein Protein Glucosinolates Meal ConcentrateConcentrate Isolate Allyl 0.21 0 0 0 (μmoles/g) 3-butenyl 12.64 0.110.23 0.17-0.41 (μmoles/g) 4-pentenyl 0.86 0 0 0 (μmoles/g)2-OH-3-butenyl 1.53 0 0 0 (μmoles/g) CH3- 0 0 0 0 thiobutenyl (μmoles/g)Phenylethyl 0.33 0 0 0 (μmoles/g) 3-CH3-indolyl 0.91 0 0 0 (μmoles/g)4-OH-3-CH3- 3.26 0 0 0 indolyl (μmoles/g) Total 15.05 0.11 0.230.17-0.41 Aliphatics (μmoles/g)

TABLE 36 Results of Proximate Analysis for Defatted Juncea Meal, ProteinEnriched Meal, Fiber Enriched Meal, Protein Concentrate and HydrolyzedCanola Protein Concentrate Crude Moisture Protein Ash Oil Fiber Sample(%) (%, dwb^(a)) (%, dwb^(a)) (%, dwb^(a)) (%, dwb^(a)) Defatted 6.4348.0 7.50 2.15 7.75 Juncea Meal Protein 5.92 51.5 7.71 1.23 5.48Enriched Meal Fiber 6.12 45.0 7.42 2.33 8.86 Enriched Meal Protein 7.8368.2 8.56 0.10 5.71 Concentrate Hydrolyzed 8.69 82.0 5.84 0.11 0.12Protein Concentrate ^(a)dwb = dry weight basis

TABLE 37 Results of Proximate Analysis of Ethanol Washed Protein SolidsCrude Solids Protein Ash Oil Fiber Sample (%) (%, dwb^(a)) (%, dwb^(a))(%, dwb^(a)) (%, dwb^(a)) Ethanol 14.07 61.4 8.26 0.74 5.53 WashedProtein Solids #1 Ethanol 19.22 66.3 8.43 0.53 5.81 Washed ProteinSolids #2 Ethanol 19.39 67.8 8.38 0.41 5.97 Washed Protein Solids #3Protein 92.17 68.2 8.56 0.10 5.71 Concentrate ^(a)dwb = dry weight basis

TABLE 38 Protein Recovery Yield Through Protein Hydrolysis and MembranePurification Solid Protein Weight Content Protein Weight Sample (kg) (%)(%, dwb) (kg, dwb) Insoluble Fiber 126.3 13.91 46.0 8.08 Solids Soluble328 2.59 84.0 7.14 Hydrolyzed Protein Extract Hydrolyzed Protein 47.71.36 39.8 0.26 Retentate from UF Hydrolyzed Protein 540 — — 6.88Permeate

TABLE 39 Results of Absorbance and Transmittance for Hydrolyzed CanolaProtein concentrate, Soy and Pea Protein Isolate Solutions at 720 nmWavelength Percent Sample Absorbance Transmittance Transmittance 1%Hydrolyzed Protein 0.014 0.97 97 Concentrate Solution 3% HydrolyzedProtein 0.053 0.89 89 Concentrate Solution 5% Hydrolyzed Protein 0.0630.87 87 Concentrate Solution 1% Soy Protein Isolate >3.8 <0.00016 <0.016Solution 1% Pea Protein Isolate >3.8 <0.00016 <0.016 Solution

TABLE 40 Mass Balance Data for Crushing and Extraction of Regular andJuncea Canola Seeds 10 kg of Regular Canola Seed 499 kg of Juncea Seed(B. napus) (B. juncea) 6.32 kg of Press Cake 278.9 kg of Press Cake 3.26kg of Press Oil 138.1 kg of Press Oil 5.02 kg of Defatted Meal 8.23 kgof Defatted Meal from 10 kg of Press Cake 1.76 kg of Protein EnrichedMeal from 1.53 kg of Protein Enriched 4.01 kg of Defatted Meal Meal from3.52 kg of Defatted Meal 2.24 kg of Fiber Enriched Meal from 1.84 kg ofFiber Enriched 4.01 kg of Defatted Meal Meal from 3.52 kg of DefattedMeal

TABLE 41 Mass Balance Data for the Wet Fiber Separation to Remove Fiberand Prepare Canola Protein Concentrates Regular Canola Protein SlurryJuncea Protein Slurry (B. napus) (B. juncea)  0.75 kg of ProteinEnriched Meal 1 kg of Protein Enriched Meal    6 kg of Water 8 kg ofWater 1.708 kg of Total Insoluble Wet Solids 2.282 kg of Total InsolubleWet Solids 0.347 kg of Wet Fiber Solids 0.431 kg of Wet Fiber Solids19.13 kg of Sugar Extract 27.32 kg of Sugar Extract 0.418 kg of DriedProtein Concentrate 0.544 kg of Dried Protein Concentrate

TABLE 42 Results of Proximate Analysis for Regular and Juncea DefattedMeals, and Protein and Fiber Enriched Meals Crude Protein Oil Ash CrudeMoisture (%, (%, (%, Fiber Sample (%) dwb^(a)) dwb^(a)) dwb^(a)) (%,dwb^(a)) Defatted Regular 7.11 46.8 1.04 7.35 9.90 Canola Meal DefattedJuncea Meal 7.18 48.7 0.87 7.48 7.44 Protein Enriched 6.77 51.5 0.517.52 7.09 Regular Canola Meal Protein Enriched 6.54 52.8 0.34 7.55 5.36Juncea Meal Fiber Enriched 7.03 43.9 1.61 7.09 13.3 Regular Canola MealFiber Enriched Juncea 6.73 45.6 1.06 7.12 9.71 Meal ^(a)dwb = dry weightbasis

TABLE 43 Results of Proximate Analysis for Regular and Juncea ProteinConcentrates and Fiber Fraction from Wet Separation Process Crude CrudeOil Ash Fiber Moisture Protein (%, (%, (%, Sample (%) (%, dwb^(a))dwb^(a)) dwb^(a)) dwb^(a)) Regular Canola 5.26 66.9 0.21 7.83 7.30Protein Concentrate Juncea Canola Protein 3.90 71.2 0.13 7.99 5.96Concentrate Regular Canola Fiber 6.74 36.3 1.52 5.83 21.6 FractionJuncea Fiber Fraction 5.68 48.2 1.41 7.91 11.49 ^(a)dwb = dry weightbasis

TABLE 44 Amino Acid Profiles of Canola Protein Concentrates and MethylPentane Defatted Regular Canola and Juncea Meals on a Normalized Basisof Pure Protein. Defatted Defatted Regular Regular Juncea Canola JunceaCanola Meal Meal Protein Protein Amino Acid (B. napus) (B. juncea)Concentrate Concentrate Aspartic Acid 6.86 7.55 6.75 7.17 (%) GlutamicAcid 18.93 19.00 19.27 18.78 (%) Serine (%) 5.03 5.15 4.95 4.95 Glycine(%) 5.45 5.48 5.40 5.41 Histidine^(a) (%) 2.77 2.21 2.39 2.39 Arginine(%) 7.78 7.71 7.29 8.22 Threonine^(a) (%) 3.86 4.24 3.89 4.10 Alanine(%) 4.90 5.00 4.81 4.88 Proline (%) 7.15 6.47 6.80 6.27 Tyrosine (%)3.62 3.66 3.79 3.96 Valine^(a) (%) 5.45 5.30 5.28 5.22 Methionine^(a)2.24 2.04 2.34 2.11 (%) Cystine (%) 2.64 2.32 2.30 2.11 Isoleucine^(a)(%) 3.88 4.18 3.96 4.08 Leucine^(a) (%) 7.34 7.66 7.68 7.91Phenylalanine^(a) 4.25 4.50 4.55 4.65 (%) Lysine^(a) (%) 6.73 6.26 6.966.27 Tryptophan^(a) 1.05 1.41 1.45 1.54 (%) Total Amino 100 100 100 100Acid (%) ^(a)Nine essential amino acids.

TABLE 45 Results of Solubility Test on Defatted Canola Meals, ProteinConcentrates, and Commercial Samples of Soy and Pea Protein IsolatesBorate-phosphate buffer (12.20 g/L of NaH₂PO₄•H₂O and 8.91 g/L ofNa₂B₄O₇•10H₂O), 1% concentration, pH 6.7, Test Method 39° C., 1 hourProtein Solubility of Defatted 31.48 Regular Canola Meal (B. napus) (%,w/w) Protein Solubility of Defatted 30.36 Juncea Meal (B. juncea) (%,w/w) Protein Solubility of Regular 36.76 Canola Protein Concentrate (%,w/w) Protein Solubility of Juncea 32.27 Protein Concentrate (%, w/w)Protein Solubility of 22.90 Commercial Soy Protein Isolate (%, w/w)Protein Solubility of 15.93 Commercial Pea Protein Isolate (%, w/w)

TABLE 46 Results of Anti-nutritional Factors. Phytate Sinapine BetainCholine (IP5 & IP6) Sample (%) (%) (%) (%, as is) Defatted Regular 0.1880.592 0.252 3.35 Canola Meal (B. napus) Defatted Juncea 0.784 0.3850.214 3.24 Meal (B. juncea) Regular Canola 0.073 0.003 0.003 4.46Protein Concentrate Juncea Protein 0.050 0.001 0.004 4.67 ConcentrateJuncea Protein 0.105 0.004 0.051 1.01 Isolate Soy Protein Isolate 0.0630.002 0.047 2.14 Pea Protein Isolate 0.058 0.004 0.010 2.43

TABLE 47 Results of Proximate Analysis for Defatted Juncea Meal andProtein Concentrate Crude Moisture Protein Ash Oil Fiber Sample (%) (%,dwb^(a)) (%, dwb^(a)) (%, dwb^(a)) (%, dwb^(a)) Defatted 6.43 48.0 7.502.15 7.75 Juncea Meal Canola 5.02 73.3 9.44 0.51 3.78 ProteinConcentrate ^(a)dwb = dry weight basis

TABLE 48 Results of Proximate Analysis for Canola Protein SlurriesContaining Soluble and Insoluble Proteins, Canola Fiber Solids, WashedCanola Fiber Solids and Insoluble Protein Solids Crude Solids ProteinAsh Oil Fiber Sample (%) (%, dwb^(a)) (%, dwb^(a)) (%, dwb^(a)) (%,dwb^(a)) Insoluble Protein Solids 6.31 52.6 8.84 0.61 1.38 and SolubleProtein Extract #1A Insoluble Protein Solids 8.81 55.4 9.06 0.29 3.32and Soluble Protein Extract #2A Insoluble Protein Solids 9.87 55.0 8.910.39 1.94 and Soluble Protein Extract #3A Insoluble Protein Solids 9.6355.5 8.71 0.39 1.44 and Soluble Protein Extract #4A Insoluble ProteinSolids 12.46 54.4 7.1 0.38 1.93 and Soluble Protein Extract #5AInsoluble Protein Solids 12.04 57.6 8.86 1.01 1.60 and Soluble ProteinExtract #6A Insoluble Fiber Solids 16.65 44.9 6.97 2.85 9.58 #1AInsoluble Fiber Solids 19.02 45.1 7.35 3.22 10.23 #2A Insoluble FiberSolids 17.54 46.6 7.79 2.34 8.04 #3A Insoluble Fiber Solids 20.46 43.47.10 3.17 10.64 #4A Insoluble Fiber Solids 20.32 44.4 7.46 2.29 9.17 #5AInsoluble Fiber Solids 20.04 44.8 7.38 3.22 10.16 #6A Insoluble ProteinSolids 1.90 49.1 12.05 0.45 0.48 and Soluble Protein Extract #1BInsoluble Protein Solids 6.12 52.9 9.14 0.46 2.00 and Soluble ProteinExtract #2B Insoluble Protein Solids 5.32 55.5 10.64 0.68 2.72 andSoluble Protein Extract #3B Insoluble Protein Solids 6.56 50.8 9.15 0.491.75 and Soluble Protein Extract #4B Insoluble Protein Solids 3.94 51.210.0 0.19 0.19 and Soluble Protein Extract #5B Insoluble Protein Solids5.60 56.8 10.05 1.53 1.35 and Soluble Protein Extract #6B Washed FiberSolids 17.28 43.1 5.45 3.08 14.23 #1B Washed Fiber Solids 18.34 43.06.01 3.52 12.93 #2B Washed Fiber Solids 17.92 43.8 6.33 3.69 13.19 #3BWashed Fiber Solids 18.23 41.6 6.46 3.39 14.09 #4B Washed Fiber Solids20.71 40.9 6.20 4.26 13.97 #5B Washed Fiber Solids 17.68 41.0 6.26 3.9010.6 #6B Soluble and Insoluble 4.34 53.4 10.0 0.60 1.57 Protein Slurry#1C Soluble and Insoluble 6.83 53.2 9.66 0.43 2.20 Protein Slurry #2CSoluble and Insoluble 5.89 53.6 9.20 0.30 9.00 Protein Slurry #3CSoluble and Insoluble 7.97 53.4 8.98 0.29 1.17 Protein Slurry #4CSoluble and Insoluble 9.03 53.9 8.83 0.77 2.02 Protein Slurry #5CInsoluble Protein Solids #1C 10.57 44.2 6.20 2.52 12.74 InsolubleProtein Solids 8.49 48.2 7.56 1.63 7.08 #2C Insoluble Protein Solids8.41 49.1 7.51 1.72 6.80 #3C Insoluble Protein Solids 15.27 43.8 7.532.86 10.79 #4C Insoluble Protein Solids 11.39 50.0 7.65 2.19 4.98 #5C^(a)dwb = dry weight basis

TABLE 49 Results of Proximate Analysis for Ethanol Precipitated andWashed Protein Solids Crude Solids Protein Ash Oil Fiber Sample (%) (%,dwb^(a)) (%, dwb^(a)) (%, dwb^(a)) (%, dwb^(a)) Ethanol 29.66 69.3 8.900.76 4.76 Precipitated Protein Solids #1 Ethanol 30.67 70.6 9.17 0.604.10 Washed Protein Solids #2 Ethanol 47.53 73.3 9.44 0.51 3.78 WashedProtein Solids #3 ^(a)dwb = dry weight basis

TABLE 50 Conditions of Andritz Decanter Centrifuge for Fiber SeparationBowl Scroll Bowl Speep G Force Differential Torque Torque Batch (RPM)(g) Speed (RPM) (%) (%) 1 1,235 274 10 34 7 2 1,226 274 14 34 10 3 1,350350 14 34 11 4 1,350 350 14 34 11 5 1,350 350 14 34 11 6 1,350 350 14 3411 7 1,350 350 14 34 11

TABLE 51 Results of Proximate Analysis for Production of ProteinConcentrate from Defatted Canola Meal % Protein % Ash % Oil % CrudeSample % Solids (dwb) (dwb) (dwb) Fiber (dwb) Defatted 93.16 48.6 7.472.45 6.98 Canola Meal Fiber Solids - 18.42 41.6 6.28 3.78 12.68 batch 1Fiber Solids - 18.06 41.2 6.28 3.57 12.80 Batch 2 Fiber Solids - 18.8841.2 6.19 3.79 12.14 Batch 3 Fiber Solids - 19.42 41.1 6.16 3.65 13.53Batch 4 Fiber Solids - 19.88 41.0 6.25 4.06 14.03 Batch 5 Fiber Solids -19.25 41.1 6.19 3.13 13.58 Batch 6 Fiber Solids - 18.84 41.0 6.13 3.1413.30 Batch 7 Protein 7.01 52.1 8.45 0.80 2.60 Slurry - Batch 1 Protein7.34 53.9 9.30 0.91 2.95 Slurry - Batch 2 Protein 7.31 54.2 8.70 0.812.83 Slurry - Batch 3 Protein 7.25 53.4 8.68 1.09 3.21 Slurry - Batch 4Protein 7.34 53.1 8.56 1.16 3.01 Slurry - Batch 5 Protein 7.22 52.8 8.501.48 3.28 Slurry - Batch 6 Protein 6.24 52.9 8.62 1.44 2.83 Slurry -Batch 7 Precipitated 16.56 65.9 8.27 0.76 4.54 Proteins - Batch 1Precipitated 4.71 63.9 8.35 0.76 4.98 Proteins - Batch 2 Precipitated18.74 63.9 8.27 0.81 5.22 Proteins - Batch 3 Precipitated 4.38 63.8 8.631.14 4.13 Proteins - Batch 4 Precipitated 4.08 65.3 8.79 1.21 4.26Proteins - Batch 5 Precipitated 16.92 64.9 8.31 0.89 4.90 Proteins -Batch 6 Precipitated 4.52 67.4 8.81 0.72 4.06 Proteins - Batch 7 Dried95.15 69.2 8.03 0.29 6.33 Protein Concentrate - Batch 1 Dried 94.67 71.69.76 0.46 5.26 Protein Concentrate - Batch 2 Dried 93.69 71.7 9.10 0.484.81 Protein Concentrate - Batch 3 Dried 93.34 72.0 8.97 0.79 4.83Protein Concentrate - Batch 4 Dried 95.74 72.1 8.98 0.78 4.64 ProteinConcentrate - Batch 5 Dried 96.89 70.3 8.65 0.74 4.88 ProteinConcentrate - Batch 6 Dried 94.32 72.7 9.13 0.64 4.31 ProteinConcentrate - Batch 7

1. A protein concentrate having a protein content of at least 60% andless than 90% protein comprising: i) a first protein fraction comprisingbetween 30% and 70% 2S protein; and ii) a second protein fractioncomprising between 20% and 50% 12S protein.
 2. The protein concentrateaccording to claim 1, wherein the first protein fraction comprisesbetween 45% and 55% 2S protein and the second protein fraction comprisesbetween 35% and 40% 12S protein.
 3. A protein isolate having a proteincontent of at least 90% protein comprising: i) a first protein fractioncomprising between 10% and 40% 2S protein; and ii) a second proteinfraction comprising between 30% and 70% 12S protein.
 4. The proteinisolate according to claim 3, wherein the first protein fractioncomprises between 15% and 30% 2S protein and the second protein fractioncomprises between 50% and 60% 12 S protein.
 5. A process for theproduction of a protein concentrate from an oilseed meal comprising: i)mixing the oilseed meal with a first blending solvent to form a mixture;ii) optionally treating the mixture with phytase at a temperature and apH suitable for phytase activity; iii) optionally adjusting the pH ofthe mixture to a pH between 6.0 and 10.0; iv) subjecting the mixture toa g-force sufficient to separate the mixture to form a) a fiberfraction, and b) protein fractions comprising an insoluble proteinfraction and a soluble protein fraction; v) optionally separating thefiber fraction from the protein fractions and mixing the fiber fractionwith a second blending solvent and repeating step iv); vi) optionallyadjusting the pH of the protein fraction to a pH between 4.0 and 6.0;vii) optionally heating the protein fraction to a temperature between80° C. and 100° C. to precipitate the proteins; and viii) separating theprecipitated proteins from the protein fraction to form the proteinconcentrate.
 6. The process according to claim 5, wherein the first andsecond blending solvents comprise water, a saline solution or apolysaccharide solution.
 7. The process according to claim 6, whereinthe first and second blending solvents comprise water.
 8. The processaccording to claim 5, the ratio of the oilseed meal to the firstblending solvent is 1:3 to 1:30 (w/w) of meal to water.
 9. The processaccording to claim 5, wherein the phytase is added in an amount between0.01% to 0.1% (w/w) based on the weight of the oilseed meal.
 10. Theprocess according to claim 5, wherein the temperature suitable forphytase activity is between 20° and 60° C.
 11. The process according toclaim 5, wherein the pH suitable for phytase activity is between 2.0 and7.0.
 12. The process according to claim 5, wherein the mixture issubjected to a g-force of between 100 g and 500 g.
 13. The processaccording to claim 12, wherein the mixture is subjected to a g-force ofbetween 150 g and 400 g.
 14. The process according to claim 13, whereinthe mixture is subjected to a g-force of between 180 g and 350 g. 15.The process according to claim 5, wherein separating the mixturecomprises using a centrifuge or a hydrocyclone.
 16. The processaccording to claim 15, wherein separating the mixture comprises using adecanter centrifuge or a disc stack centrifuge.
 17. The processaccording to claim 5, wherein separating the precipitated proteinscomprises using a centrifuge or a hydrocyclone.
 18. The processaccording to claim 17, wherein centrifuging the precipitated proteinscomprises a g-force between 2,500 g and 9,500 g.
 19. The processaccording to claim 5, further comprising the step of drying the proteinconcentrate to a moisture of between 4% and 8% (w/w).
 20. The processaccording to claim 5, wherein the protein concentrate also comprisespeptides and free amino acids.
 21. The process according to claim 5,wherein the protein concentrate is hydrolyzed to produce peptides andfree amino acids.
 22. The process according to claim 5, wherein theoilseed meal comprises a canola, rapeseed, mustard seed, broccoli seed,flax seed, cotton seed, hemp seed, safflower seed, sesame seed orsoybean meal.
 23. The process according to claim 22, wherein the oilseedmeal comprises canola meal.
 24. A process for the production of aprotein concentrate from an oilseed meal comprising: i) mixing theoilseed meal with a first blending solvent to form a mixture; ii)optionally treating the mixture with phytase at a temperature and a pHsuitable for phytase activity; iii) optionally adjusting the pH of themixture to a pH between 6.0 and 10.0; iv) subjecting the mixture to ag-force sufficient to separate the mixture to form a) a fiber fraction,and b) protein fractions comprising an insoluble protein fraction and asoluble protein fraction; v) optionally separating the fiber fractionfrom the protein fractions and mixing the fiber fraction with a secondblending solvent and repeating step iv); vi) optionally adjusting the pHof the protein fraction to a pH between 4.0 and 6.0; vii) mixing theprotein fraction with a mixing solvent to form a protein slurry andprecipitate the proteins; viii) separating the precipitated proteinsfrom the protein slurry to form the protein concentrate; and ix)optionally repeating steps vii) and viii) with the precipitatedproteins.
 25. The process according to claim 24, wherein the first andsecond blending solvents comprise water, a saline solution or apolysaccharide solution.
 26. The process according to claim 25, whereinthe first and second blending solvents comprise water.
 27. The processaccording to claim 24, the ratio of the oilseed meal to the firstblending solvent is 1:3 to 1:30 (w/w) of meal to water.
 28. The processaccording to claim 24, wherein the phytase is added in an amount between0.01% and 0.1% (w/w) based on the weight of the oilseed meal.
 29. Theprocess according to claim 24, wherein the temperature suitable forphytase activity is between 20° and 60° C.
 30. The process according toclaim 24, wherein the pH suitable for phytase activity is between 2.0and 7.0.
 31. The process according to claim 24, wherein the mixture issubjected to a g-force of between 100 g and 500 g.
 32. The processaccording to claim 31, wherein the mixture is subjected to a g-force ofbetween 150 g and 400 g.
 33. The process according to claim 32, whereinthe mixture is subjected to a g-force of between 180 g and 350 g. 34.The process according to claim 24, wherein separating the mixturecomprises using a centrifuge or a hydrocyclone.
 35. The processaccording to claim 34, wherein the centrifuge comprises a decantercentrifuge or a disc stack centrifuge.
 36. The process according toclaim 24, wherein the mixing solvent comprises an ethanol:water mixture,wherein the ethanol is present in an amount between 80% and 100% (v/v).37. The process according to claim 24, wherein separating theprecipitated proteins comprises using a centrifuge or a hydrocyclone.38. The process according to claim 37, wherein centrifuging theprecipitated proteins comprises a g-force between 2,500 g and 9,500 g.39. The process according to claim 24, wherein steps viii) and viii) arerepeated at least twice.
 40. The process according to claim 24, furthercomprising the step of drying the protein concentrate to a moisture ofbetween 4% and 8% (w/w).
 41. The process according to claim 24, whereinthe protein concentrate also comprises peptides and amino acids.
 42. Theprocess according to claim 24, wherein the protein concentrate ishydrolyzed to produce peptides and free amino acids.
 43. The processaccording to claim 24, wherein the oilseed meal comprises a canola,rapeseed, mustard seed, broccoli seed, flax seed, cotton seed, hempseed, safflower seed, sesame seed or soybean meal.
 44. The processaccording to claim 43, wherein the oilseed meal comprises canola meal.45. A process for the production of a protein isolate from an oilseedmeal comprising: i) mixing the oilseed meal with a first blendingsolvent to form a mixture; ii) optionally treating the mixture withphytase at a temperature and a pH suitable for phytase activity; iii)optionally adjusting the pH of the mixture to a pH between 6.0 and 10.0;iv) subjecting the mixture to a g-force sufficient to separate themixture to form a) a fiber fraction, and b) protein fractions comprisingan insoluble protein fraction and a soluble protein fraction; v)optionally separating the fiber fraction from the protein fractions andmixing the fiber fraction with a second blending solvent and repeatingstep iv); vi) separating the insoluble protein fraction from the solubleprotein fraction to recover therefrom an insoluble protein concentrateand a soluble protein extract; and vii) subjecting the soluble proteinextract to filtration to recover therefrom the protein isolate.
 46. Theprocess according to claim 45, wherein the first and second blendingsolvents comprise water, a saline solution or a polysaccharide solution.47. The process according to claim 46, wherein the first and secondblending solvents comprise water.
 48. The process according to claim 45,the ratio of the oilseed meal to the first blending solvent is 1:3 to1:30 (w/w) of meal to water.
 49. The process according to claim 45,wherein the phytase is added in an amount between 0.01% to 0.1% (w/w)based on the weight of the oilseed meal.
 50. The process according toclaim 45, wherein the temperature suitable for enzymatic activity isbetween 20° and 60° C.
 51. The process according to claim 45, whereinthe pH suitable for enzymatic activity is between 2.0 and 7.0.
 52. Theprocess according to claim 45, wherein the mixture is subjected to ag-force of between 100 g and 500 g.
 53. The process according to claim52, wherein the mixture is subjected to a g-force of between 150 g and350 g.
 54. The process according to claim 53, wherein the mixture issubjected to a g-force of between 180 g and 350 g.
 55. The processaccording to claim 45, wherein separating the mixture comprises using acentrifuge or a hydrocyclone.
 56. The process according to claim 55,wherein the centrifuge comprises a decanter centrifuge or a disc stackcentrifuge.
 57. The process according to claim 56, wherein separatingthe insoluble fiber fraction from the soluble fiber fraction comprisesusing a centrifuge or a hydrocyclone.
 58. The process according to claim57, wherein centrifuging to separate the insoluble fiber fraction fromthe soluble fiber fraction comprises a g-force between 2,500 g and 9,500g.
 59. The process according to claim 45, further comprising the step ofdrying the protein isolate to a moisture of between 4% and 8% (w/w). 60.The process according to claim 45, wherein the protein isolate alsocomprises peptides and amino acids.
 61. The process according to claim45, wherein the protein isolate is hydrolyzed to produce peptides andfree amino acids.
 62. The process according to claim 45, wherein theoilseed meal comprises a canola, rapeseed, mustard seed, broccoli seed,flax seed, cotton seed, hemp seed, safflower seed, sesame seed orsoybean meal.
 63. The process according to claim 62, wherein the oilseedmeal comprises canola meal.